OJS · Class I — Low Risk (general controls) · General, Plastic Surgery · 21 CFR 878.5900
Classification
FDA Product Code
OJS
Device class
Class I — Low Risk (general controls)
Regulation
21 CFR 878.5900
Review panel
SU
Medical specialty
General, Plastic Surgery
Submission type
7
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N
Definition
This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance