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DENTAL, MEDICAL INSTRUMENT CASES & CASSETTE

K962545 Class II Traditional
Decision Date
1997-03-07
Sponsor / Applicant
Sterilization Cassette Systems, Inc.

Technical Specification

510(k) Submission ID K962545
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1997-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTAL, MEDICAL INSTRUMENT CASES & CASSETTE received FDA 510(k) clearance under submission number K962545, sponsored by Sterilization Cassette Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1997-03-07.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.