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BONDING AGENT, PRESTIGE

K760324 Class II Traditional
Decision Date
1976-08-03
Sponsor / Applicant
Lee Pharmaceuticals

Technical Specification

510(k) Submission ID K760324
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1976-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BONDING AGENT, PRESTIGE received FDA 510(k) clearance under submission number K760324, sponsored by Lee Pharmaceuticals. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1976-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.