INTEGRAPH FLASH, MODEL CI 110— 510(k) K012732

Substantially Equivalent

Steritec Products, Inc.

FDA 510(k) clearance K012732 for INTEGRAPH FLASH, MODEL CI 110, Substantially Equivalent on 2002-03-04. Applicant: Steritec Products, Inc..

Clearance details

Applicant: Steritec Products, Inc.
Product code: Code JOJ
Advisory panel: General Hospital
Date received: 2001-08-16
Decision date: 2002-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Castle Rock, CO, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.