meddevicedb.com FDA Device Reference

PRIMODENT ACRYLIC TEETH

K926070 Class II Traditional
Decision Date
1994-02-17
Sponsor / Applicant
I.T.C. Ent.

Technical Specification

510(k) Submission ID K926070
Product Code ELM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3590
Decision Date 1994-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRIMODENT ACRYLIC TEETH received FDA 510(k) clearance under submission number K926070, sponsored by I.T.C. Ent.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-02-17.

Classification & Regulation

This clearance is catalogued under FDA product code ELM and 21 CFR 872.3590, within the Dental review panel as a Class II device.