VERIFY BIOLOGICAL INDICATOR CHALLENGE PACK FOR VAPORIZED VH202 STERILIZATION— 510(k) K092906

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K092906 for VERIFY BIOLOGICAL INDICATOR CHALLENGE PACK FOR VAPORIZED VH202 STERILIZATION, Substantially Equivalent on 2009-12-30. Applicant: STERIS Corporation. Device class: 2.

Clearance details

Applicant
STERIS Corporation
Product code
Code FRC
Device class
Class 2
Regulation
21 CFR 880.2800
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mentor, OH, US
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