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S.S. WHITE-PENNWALT RENEW CALCIUM HYDROX

K801860 Class II Traditional
Decision Date
1980-10-10
Sponsor / Applicant
Pennwalt Corp.

Technical Specification

510(k) Submission ID K801860
Product Code EJK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3250
Decision Date 1980-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S.S. WHITE-PENNWALT RENEW CALCIUM HYDROX received FDA 510(k) clearance under submission number K801860, sponsored by Pennwalt 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 1980-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code EJK and 21 CFR 872.3250, within the Dental review panel as a Class II device.