N.M. Admin. Code § 16.19.14.9 - ADULTERATION
A device may be considered to be adulterated:
A. It is subject to a performance standard
and does not comply with all requirements of such standard.
B. Class II device FDA pre-market approval is
not completed.
C. It is a banned
device.
D. It is in violation of
good manufacturing practice requirements.
E. It fails to comply with the IDE
(Investigational Device Exemption) protocol.
Notes
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.