Current through Register Vol. 35, No. 21, November 5, 2024
Section 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.N.M. Admin. Code § 16.19.14.9
03-07-80...08-27-90; 16.19.14.9 NMAC - Rn, 16 NMAC 19.14.9, 03-30-02, Adopted by New Mexico Register, Volume XXXIV, Issue 04, February 28, 2023, eff. 2/28/2023