MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT— 510(k) K910022

Name: FDA 510(k) clearance K910022
Creator: U.S. Food and Drug Administration
Published: 1991-04-02

Unknown

Medical Marketing Group

FDA 510(k) clearance K910022 for MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT, Unknown on 1991-04-02. Applicant: Medical Marketing Group. Device class: 2.

Clearance details

Applicant: Medical Marketing Group
Product code: Code FCM
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1991-01-03
Decision date: 1991-04-02
Decision: Unknown
Clearance type: Traditional
Location: Decatur, GA, US

Download summary PDF View on FDA.gov ↗

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