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THERACAL LC

K063237 Class II Traditional
Decision Date
2006-12-08
Sponsor / Applicant
Bisco, Inc.

Technical Specification

510(k) Submission ID K063237
Product Code EJK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3250
Decision Date 2006-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERACAL LC received FDA 510(k) clearance under submission number K063237, sponsored by Bisco, 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 2006-12-08.

Classification & Regulation

This clearance is catalogued under FDA product code EJK and 21 CFR 872.3250, within the Dental review panel as a Class II device.