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SEPTOCALCINE ULTRA

K920692 Class II Traditional
Decision Date
1992-04-21
Sponsor / Applicant
Specialites Septodont

Technical Specification

510(k) Submission ID K920692
Product Code EJK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3250
Decision Date 1992-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SEPTOCALCINE ULTRA received FDA 510(k) clearance under submission number K920692, sponsored by Specialites Septodont. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1992-04-21.

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.