STERITEC INTEGRAPH MODEL CI-101— 510(k) K960441

Substantially Equivalent

Steritec Products Mfg Co, Inc.

FDA 510(k) clearance K960441 for STERITEC INTEGRAPH MODEL CI-101, Substantially Equivalent on 1997-05-08. Applicant: Steritec Products Mfg Co, Inc..

Clearance details

Applicant: Steritec Products Mfg Co, Inc.
Product code: Code JOJ
Advisory panel: General Hospital
Date received: 1996-02-01
Decision date: 1997-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aurora, CO, US

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