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PART 872 DEGUFILL H & DEGUFILL M DA

K914368 Class I Traditional
Decision Date
1991-11-13
Sponsor / Applicant
Degussa AG

Technical Specification

510(k) Submission ID K914368
Product Code EKJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1991-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PART 872 DEGUFILL H & DEGUFILL M DA received FDA 510(k) clearance under submission number K914368, sponsored by Degussa AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code EKJ and 21 CFR 872.4565, within the Dental review panel as a Class I device.