VERIFY V-PRO CHEMICAL INDICATOR, VERSIONS 1 AND 2— 510(k) K072510

Name: FDA 510(k) clearance K072510
Creator: U.S. Food and Drug Administration
Published: 2007-12-11

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K072510 for VERIFY V-PRO CHEMICAL INDICATOR, VERSIONS 1 AND 2, Substantially Equivalent on 2007-12-11. 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: 2007-09-06
Decision date: 2007-12-11
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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