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UNI-BITE DENTAL X-RAY FILM HOLDER

K813378 Class I Traditional
Decision Date
1982-01-29
Sponsor / Applicant
Rinn Corp.

Technical Specification

510(k) Submission ID K813378
Product Code EGZ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1905
Decision Date 1982-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNI-BITE DENTAL X-RAY FILM HOLDER received FDA 510(k) clearance under submission number K813378, sponsored by Rinn Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1982-01-29.

Classification & Regulation

This clearance is catalogued under FDA product code EGZ and 21 CFR 872.1905, within the Dental review panel as a Class I device.