meddevicedb.com FDA Device Reference

CIMPAT (PINK AND WHITE)

K761354 Class II Traditional
Decision Date
1977-01-03
Sponsor / Applicant
Septodont, Inc.

Technical Specification

510(k) Submission ID K761354
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 1977-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIMPAT (PINK AND WHITE) received FDA 510(k) clearance under submission number K761354, sponsored by Septodont, 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 1977-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.