OGG · Class II — Moderate Risk (510(k) clearance required) · Anesthesiology · 21 CFR 868.5450
Classification
FDA Product Code
OGG
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 868.5450
Review panel
AN
Medical specialty
Anesthesiology
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 kit, as described in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market.