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ELASTIC MANDIBULAR ADVANCEMENT - TITRATION (EMA-T) APPILANCE

K973884 Class II Traditional
Decision Date
1998-01-09
Sponsor / Applicant
Frantz Design, Inc.

Technical Specification

510(k) Submission ID K973884
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 1998-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELASTIC MANDIBULAR ADVANCEMENT - TITRATION (EMA-T) APPILANCE received FDA 510(k) clearance under submission number K973884, sponsored by Frantz Design, 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 1998-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code LRK and 21 CFR 872.5570, within the Dental review panel as a Class II device.