VERIFY V-PRO CHEMICAL INDICATOR, VERSION 1A: VERIFY V-PRO CHEMICAL INDICATOR; VERSION 2A: ADHESIVE LABEL— 510(k) K091174

Name: FDA 510(k) clearance K091174
Creator: U.S. Food and Drug Administration
Published: 2009-10-27

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K091174 for VERIFY V-PRO CHEMICAL INDICATOR, VERSION 1A: VERIFY V-PRO CHEMICAL INDICATOR; VERSION 2A: ADHESIVE LABEL, Substantially Equivalent on 2009-10-27. Applicant: STERIS Corporation. Device class: 2.

Clearance details

Applicant: STERIS Corporation
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 2009-04-22
Decision date: 2009-10-27
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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