meddevicedb.com FDA Device Reference

P10 SPECIAL

K993344 Class II Traditional
Decision Date
1999-11-15
Sponsor / Applicant
North American Alloys, Inc.

Technical Specification

510(k) Submission ID K993344
Product Code EJH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3710
Decision Date 1999-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

P10 SPECIAL received FDA 510(k) clearance under submission number K993344, sponsored by North American Alloys, 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 1999-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code EJH and 21 CFR 872.3710, within the Dental review panel as a Class II device.