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APPLICATOR, LEE IMPRESSION

K781977 Class I Traditional
Decision Date
1978-12-20
Sponsor / Applicant
Lee Pharmaceuticals

Technical Specification

510(k) Submission ID K781977
Product Code EID
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1978-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APPLICATOR, LEE IMPRESSION received FDA 510(k) clearance under submission number K781977, 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 1978-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code EID and 21 CFR 872.4565, within the Dental review panel as a Class I device.