BIOPSY FORCEPS— 510(k) K840818

Substantially Equivalent

American Endoscopy, Inc.

FDA 510(k) clearance K840818 for BIOPSY FORCEPS, Substantially Equivalent on 1984-04-13. Applicant: American Endoscopy, Inc..

Clearance details

Applicant: American Endoscopy, Inc.
Product code: Code FCL
Advisory panel: Gastroenterology, Urology
Date received: 1984-02-24
Decision date: 1984-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Adverse events under product code FCL

product code FCL

Death: 5
Total: 5

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.