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ACETAL DENTAL/PREFORMED CLASP

K983558 Class I Traditional
Decision Date
1999-01-07
Sponsor / Applicant
Dentamax, Inc.

Technical Specification

510(k) Submission ID K983558
Product Code EHP
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3285
Decision Date 1999-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACETAL DENTAL/PREFORMED CLASP received FDA 510(k) clearance under submission number K983558, sponsored by Dentamax, 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 1999-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code EHP and 21 CFR 872.3285, within the Dental review panel as a Class I device.