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FOGCUTTER DENTAL MOUTH MIRROR

K833310 Class I Traditional
Decision Date
1984-05-07
Sponsor / Applicant
Hti, Inc.

Technical Specification

510(k) Submission ID K833310
Product Code EAX
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1984-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FOGCUTTER DENTAL MOUTH MIRROR received FDA 510(k) clearance under submission number K833310, sponsored by Hti, 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 1984-05-07.

Classification & Regulation

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