VERIFY BIOLOGICAL INDICATOR CHALLENGE PACK FOR VAPORIZED VH202 STERILIZATION PROCESSES— 510(k) K103331

Name: FDA 510(k) clearance K103331
Creator: U.S. Food and Drug Administration
Published: 2011-09-01

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K103331 for VERIFY BIOLOGICAL INDICATOR CHALLENGE PACK FOR VAPORIZED VH202 STERILIZATION PROCESSES, Substantially Equivalent on 2011-09-01. 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: 2010-11-12
Decision date: 2011-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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