ENDPOINT 500 PERACETIC ACID TEST INDICATORS— 510(k) K931935

Name: FDA 510(k) clearance K931935
Creator: U.S. Food and Drug Administration
Published: 1994-02-07

Substantially Equivalent

Minntech Corp.

FDA 510(k) clearance K931935 for ENDPOINT 500 PERACETIC ACID TEST INDICATORS, Substantially Equivalent on 1994-02-07. Applicant: Minntech Corp.. Device class: 2.

Clearance details

Applicant: Minntech Corp.
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1993-04-19
Decision date: 1994-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.