JOSLYN EO STERILIZER/ EO MODERNIZATION KIT— 510(k) K901146

Name: FDA 510(k) clearance K901146
Creator: U.S. Food and Drug Administration
Published: 1991-03-07

Substantially Equivalent

Joslyn Valve Corp.

FDA 510(k) clearance K901146 for JOSLYN EO STERILIZER/ EO MODERNIZATION KIT, Substantially Equivalent on 1991-03-07. Applicant: Joslyn Valve Corp.. Device class: 2.

Clearance details

Applicant: Joslyn Valve Corp.
Product code: Code FLF
Device class: Class 2
Regulation: 21 CFR 880.6860
Advisory panel: General Hospital
Date received: 1990-03-12
Decision date: 1991-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Macedon, NY, US

Download summary PDF View on FDA.gov ↗

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