AN3200 DOUBILET DRAIN— 510(k) K872458

Substantially Equivalent

H.W. Andersen Products, Inc.

FDA 510(k) clearance K872458 for AN3200 DOUBILET DRAIN, Substantially Equivalent on 1987-09-21. Applicant: H.W. Andersen Products, Inc..

Clearance details

Applicant: H.W. Andersen Products, Inc.
Product code: Code FGE
Advisory panel: Gastroenterology, Urology
Date received: 1987-06-23
Decision date: 1987-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oyster Bay, NY, US

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Adverse events under product code FGE

product code FGE

Death: 52
Injury: 2,347
Malfunction: 9,798
Other: 1
Total: 12,198

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.