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DENTAL HAND INSTRUMENTS

K883322 Class I Traditional
Decision Date
1988-08-26
Sponsor / Applicant
Collagen Corp.

Technical Specification

510(k) Submission ID K883322
Product Code EKJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1988-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTAL HAND INSTRUMENTS received FDA 510(k) clearance under submission number K883322, sponsored by Collagen Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1988-08-26.

Classification & Regulation

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