VERIFY CHALLENGE PACKS, MODELS 270F 4 CHALLENGE PACK; 275F 3 CHALLENGE PACK; 275F 10 CHALLENGE PACK— 510(k) K070895

Name: FDA 510(k) clearance K070895
Creator: U.S. Food and Drug Administration
Published: 2007-09-05

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K070895 for VERIFY CHALLENGE PACKS, MODELS 270F 4 CHALLENGE PACK; 275F 3 CHALLENGE PACK; 275F 10 CHALLENGE PACK, Substantially Equivalent on 2007-09-05. 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: 2007-03-30
Decision date: 2007-09-05
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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