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WILLI GELLER CREATION & AV PORCELAIN

K002041 Class II Traditional
Decision Date
2000-08-16
Sponsor / Applicant
Jensen Industries, Inc.

Technical Specification

510(k) Submission ID K002041
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2000-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WILLI GELLER CREATION & AV PORCELAIN received FDA 510(k) clearance under submission number K002041, sponsored by Jensen Industries, 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 2000-08-16.

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.