CAZ · Class II — Moderate Risk (510(k) clearance required) · Anesthesiology · 21 CFR 868.5140
Classification
FDA Product Code
CAZ
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 868.5140
Review panel
AN
Medical specialty
Anesthesiology
Submission type
1
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
Y
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.