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REVERSIBLE HYDROCOLLOID IMPRESSION

K811020 Class II Traditional
Decision Date
1981-05-05
Sponsor / Applicant
Kottler Laboratories

Technical Specification

510(k) Submission ID K811020
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 1981-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REVERSIBLE HYDROCOLLOID IMPRESSION received FDA 510(k) clearance under submission number K811020, sponsored by Kottler Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1981-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.