INTRAVENOUS CATHETERS MODIFICATIONS— 510(k) K921295

Name: FDA 510(k) clearance K921295
Creator: U.S. Food and Drug Administration
Published: 1993-05-17

Substantially Equivalent

Critikon Company, LLC

FDA 510(k) clearance K921295 for INTRAVENOUS CATHETERS MODIFICATIONS, Substantially Equivalent on 1993-05-17. Applicant: Critikon Company, LLC. Device class: 2.

Clearance details

Applicant: Critikon Company, LLC
Product code: Code FGO
Device class: Class 2
Regulation: 21 CFR 876.4680
Advisory panel: Gastroenterology, Urology
Date received: 1992-03-12
Decision date: 1993-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, US

Download summary PDF View on FDA.gov ↗

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