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NU-CAP CALCIUM HYDROX. PULP CAPPING

K831575 Class II Traditional
Decision Date
1983-06-30
Sponsor / Applicant
Coe Laboratories, Inc.

Technical Specification

510(k) Submission ID K831575
Product Code EJK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3250
Decision Date 1983-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NU-CAP CALCIUM HYDROX. PULP CAPPING received FDA 510(k) clearance under submission number K831575, sponsored by Coe Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1983-06-30.

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.