21 CFR 801.109 - Prescription devices.
A device which, because of any potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use is not safe except under the supervision of a practitioner licensed by law to direct the use of such device, and hence for which “adequate directions for use” cannot be prepared, shall be exempt from section 502(f)(1) of the act if all the following conditions are met:
(a) The device is:
(i) In the possession of a person, or his agents or employees, regularly and lawfully engaged in the manufacture, transportation, storage, or wholesale or retail distribution of such device; or
(ii) In the possession of a practitioner, such as physicians, dentists, and veterinarians, licensed by law to use or order the use of such device; and
(2) Is to be sold only to or on the prescription or other order of such practitioner for use in the course of his professional practice.
(b) The label of the device, other than surgical instruments, bears:
(1) The symbol statement “Rx only” or “℞ only” or the statement “Caution: Federal law restricts this device to sale by or on the order of a ___”, the blank to be filled with the word “physician”, “dentist”, “veterinarian”, or with the descriptive designation of any other practitioner licensed by the law of the State in which the practitioner practices to use or order the use of the device; and
(2) The method of its application or use.
(c) Labeling on or within the package from which the device is to be dispensed bears information for use, including indications, effects, routes, methods, and frequency and duration of administration, and any relevant hazards, contraindications, side effects, and precautions under which practitioners licensed by law to administer the device can use the device safely and for the purpose for which it is intended, including all purposes for which it is advertised or represented: Provided, however, That such information may be omitted from the dispensing package if, but only if, the article is a device for which directions, hazards, warnings, and other information are commonly known to practitioners licensed by law to use the device. Upon written request, stating reasonable grounds therefor, the Commissioner will offer an opinion on a proposal to omit such information from the dispensing package under this proviso.
(d) Any labeling, as defined in section 201(m) of the act, whether or not it is on or within a package from which the device is to be dispensed, distributed by or on behalf of the manufacturer, packer, or distributor of the device, that furnishes or purports to furnish information for use of the device contains adequate information for such use, including indications, effects, routes, methods, and frequency and duration of administration and any relevant hazards, contraindications, side effects, and precautions, under which practitioners licensed by law to employ the device can use the device safely and for the purposes for which it is intended, including all purposes for which it is advertised or represented. This information will not be required on so-called reminder - piece labeling which calls attention to the name of the device but does not include indications or other use information.
(e) All labeling, except labels and cartons, bearing information for use of the device also bears the date of the issuance or the date of the latest revision of such labeling.
Title 21 published on 10-May-2017 03:43
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR Part 801 after this date.
- 21 CFR 872.1870 — Sulfide Detection Device.
- 21 CFR 882.1935 — Near Infrared (NIR) Brain Hematoma Detector.
- 21 CFR 801.125 — Medical Devices for Use in Teaching, Law Enforcement, Research, and Analysis.
- 21 CFR 801.110 — Retail Exemption for Prescription Devices.
- 21 CFR 882.5970 — Cranial Orthosis.
- 21 CFR 880.5130 — Infant Radiant Warmer.
- 21 CFR 801.127 — Medical Devices; Expiration of Exemptions.
- 21 CFR 801.128 — Exceptions or Alternatives to Labeling Requirements for Medical Devices Held by the Strategic National Stockpile.
- 21 CFR 884.5200 — Hemorrhoid Prevention Pressure Wedge.
- 21 CFR 872.1745 — Laser Fluorescence Caries Detection Device.
- 21 CFR 801.15 — Medical Devices; Prominence of Required Label Statements; Use of Symbols in Labeling.
- 21 CFR 876.5310 — Nonimplanted, Peripheral Electrical Continence Device.
- 21 CFR 862.1118 — Biotinidase Test System.
- 21 CFR 876.1735 — Electrogastrography System.
- 21 CFR 870.3460 — Endovascular Suturing System.