PVT — Maternity Kit Class I

FDA Device Classification

FDA product code PVT covers "Maternity Kit", a Class I medical device regulated under 21 CFR 884.5435. Submissions are reviewed by the Obstetrics/Gynecology panel.

Classification Details

Product Code
PVT
Device Class
Class I
Regulation Number
884.5435
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Definition

This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. 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.