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HERACERAM PRESS

K040859 Class II Traditional
Decision Date
2004-05-20
Sponsor / Applicant
Heraeus Kulzer, Inc.

Technical Specification

510(k) Submission ID K040859
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2004-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HERACERAM PRESS received FDA 510(k) clearance under submission number K040859, sponsored by Heraeus Kulzer, 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 2004-05-20.

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.