URETHRAL CATHETERIZATION TRAY/UNIVERSAL URETHRAL CATH TRAY— 510(k) K962073

Name: FDA 510(k) clearance K962073
Creator: U.S. Food and Drug Administration
Published: 1996-06-21

Substantially Equivalent

Continental Medical Laboratories, Inc.

FDA 510(k) clearance K962073 for URETHRAL CATHETERIZATION TRAY/UNIVERSAL URETHRAL CATH TRAY, Substantially Equivalent on 1996-06-21. Applicant: Continental Medical Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Continental Medical Laboratories, Inc.
Product code: Code FCM
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1996-05-28
Decision date: 1996-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waterford, WI, US

Download summary PDF View on FDA.gov ↗

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