meddevicedb.com FDA Device Reference

PREVISION CHEM

K010541 Class II Traditional
Decision Date
2001-07-31
Sponsor / Applicant
Heraeus Kulzer, Inc.

Technical Specification

510(k) Submission ID K010541
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2001-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREVISION CHEM received FDA 510(k) clearance under submission number K010541, 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 2001-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.