21 CFR 874, Subpart D - Prosthetic Devices
- § 874.3300 — Hearing Aid.
- § 874.3305 — Wireless air-conduction hearing aid.
- § 874.3310 — Hearing aid calibrator and analysis system.
- § 874.3320 — Group hearing aid or group auditory trainer.
- § 874.3330 — Master hearing aid.
- § 874.3375 — Battery-powered artificial larynx.
- § 874.3400 — Tinnitus masker.
- § 874.3430 — Middle ear mold.
- § 874.3450 — Partial ossicular replacement prosthesis.
- § 874.3495 — Total ossicular replacement prosthesis.
- § 874.3540 — Prosthesis modification instrument for ossicular replacement surgery.
- § 874.3620 — Ear, nose, and throat synthetic polymer material.
- § 874.3695 — Mandibular implant facial prosthesis.
- § 874.3730 — Laryngeal prosthesis (Taub design).
- § 874.3760 — Sacculotomy tack (Cody tack)
- § 874.3820 — Endolymphatic shunt.
- § 874.3850 — Endolymphatic shunt tube with valve.
- § 874.3880 — Tympanostomy tube.
- § 874.3900 — Nasal dilator.
- § 874.3930 — Tympanostomy tube with semipermeable membrane.
- § 874.3950 — Transcutaneous air conduction hearing aid system.
Title 21 published on 2012-04-01
The following are only the Rules published in the Federal Register after the published date of Title 21.
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This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
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§ 360i - Records and reports on devices
Title 21 published on 2012-04-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 874 after this date.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-06826 RIN Docket No. FDA-2013-N-0011 DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration Final rule; technical amendment. This rule is effective March 26, 2013. 21 CFR Parts 814, 822, 862, 864, 866, 868, 870, 872, 874, 876, 878, 880, 882, 884, 886, 888, 890, and 892 The Food and Drug Administration (FDA) is amending certain medical device regulations to correct minor errors in the Code of Federal Regulations (CFR). This action is editorial in nature and is intended to provide accuracy and clarity to the Agency's regulations.