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PROCERA ALL-CERAMIC PORCELAIN

K944702 Class II Traditional
Decision Date
1994-12-02
Sponsor / Applicant
Nobelpharma USA, Inc.

Technical Specification

510(k) Submission ID K944702
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1994-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCERA ALL-CERAMIC PORCELAIN received FDA 510(k) clearance under submission number K944702, sponsored by Nobelpharma USA, 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 1994-12-02.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.