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IMAGINE H.E. PRESS DESIGN-CERAMIC

K020774 Class II Traditional
Decision Date
2002-05-22
Sponsor / Applicant
Wieland Dental + Technik GmbH & Co. KG

Technical Specification

510(k) Submission ID K020774
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2002-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGINE H.E. PRESS DESIGN-CERAMIC received FDA 510(k) clearance under submission number K020774, sponsored by Wieland Dental + Technik GmbH & Co. KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-05-22.

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.