MENSINK-GOOSEN CATHETER— 510(k) K844889

Name: FDA 510(k) clearance K844889
Creator: U.S. Food and Drug Administration
Published: 1985-03-18

Substantially Equivalent

Goosen Enterprises, Inc.

FDA 510(k) clearance K844889 for MENSINK-GOOSEN CATHETER, Substantially Equivalent on 1985-03-18. Applicant: Goosen Enterprises, Inc.. Device class: 1.

Clearance details

Applicant: Goosen Enterprises, Inc.
Product code: Code GBP
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1984-12-17
Decision date: 1985-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Goldenrod, FL, US

Download summary PDF View on FDA.gov ↗

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