AN3100 MULHOLLAND DRAIN— 510(k) K872459

Name: FDA 510(k) clearance K872459
Creator: U.S. Food and Drug Administration
Published: 1987-07-21

Substantially Equivalent

H.W. Andersen Products, Inc.

FDA 510(k) clearance K872459 for AN3100 MULHOLLAND DRAIN, Substantially Equivalent on 1987-07-21. Applicant: H.W. Andersen Products, Inc.. Device class: 1.

Clearance details

Applicant: H.W. Andersen Products, Inc.
Product code: Code GBS
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1987-06-23
Decision date: 1987-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oyster Bay, NY, US

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