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WILLI GELLER CREATION PORCELAIN

K981490 Class II Traditional
Decision Date
1998-10-22
Sponsor / Applicant
Jensen Industries, Inc.

Technical Specification

510(k) Submission ID K981490
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1998-10-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WILLI GELLER CREATION PORCELAIN received FDA 510(k) clearance under submission number K981490, 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 1998-10-22.

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.