NYC — Dental Prophylaxis Kit Class I

FDA Device Classification

FDA product code NYC covers "Dental Prophylaxis Kit", a Class I medical device regulated under 21 CFR 872.4565. Submissions are reviewed by the Dental panel.

Classification Details

Product Code
NYC
Device Class
Class I
Regulation Number
872.4565
Submission Type
Review Panel
DE
Medical Specialty
Dental
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.