MLT · Class II — Moderate Risk (510(k) clearance required) · Obstetrics/Gynecology · 21 CFR 884.4530
Classification
FDA Product Code
MLT
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 884.4530
Review panel
OB
Medical specialty
Obstetrics/Gynecology
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.