ABDOMINAL FLUID CONTROL POUCH, 203-301-S; ETC.— 510(k) K932857

Name: FDA 510(k) clearance K932857
Creator: U.S. Food and Drug Administration
Published: 1993-09-13

Substantially Equivalent

Ansley Medical Products, Inc.

FDA 510(k) clearance K932857 for ABDOMINAL FLUID CONTROL POUCH, 203-301-S; ETC., Substantially Equivalent on 1993-09-13. Applicant: Ansley Medical Products, Inc.. Device class: 2.

Clearance details

Device name as filed: ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.
Applicant: Ansley Medical Products, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1993-06-10
Decision date: 1993-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

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