O'NEIL URINARY CATHETER INTRODUCER— 510(k) K884819

Name: FDA 510(k) clearance K884819
Creator: U.S. Food and Drug Administration
Published: 1989-02-17

Substantially Equivalent

Medical Marketing Group

FDA 510(k) clearance K884819 for O'NEIL URINARY CATHETER INTRODUCER, Substantially Equivalent on 1989-02-17. Applicant: Medical Marketing Group. Device class: 2.

Clearance details

Applicant: Medical Marketing Group
Product code: Code KNY
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1988-11-17
Decision date: 1989-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Decatur, GA, US

Download summary PDF View on FDA.gov ↗

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