VERIFY CHEMICAL MONITORING STRIP FOR RESERT SOULTIONS (RESERT XL TEST STRIP VERSION 2)— 510(k) K102296

Name: FDA 510(k) clearance K102296
Creator: U.S. Food and Drug Administration
Published: 2011-02-09

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K102296 for VERIFY CHEMICAL MONITORING STRIP FOR RESERT SOULTIONS (RESERT XL TEST STRIP VERSION 2), Substantially Equivalent on 2011-02-09. 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: 2010-08-13
Decision date: 2011-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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