OLYMPUS FB SERIES BIOPSY FORCEPS— 510(k) K955065

Substantially Equivalent

Olympus America, Inc.

FDA 510(k) clearance K955065 for OLYMPUS FB SERIES BIOPSY FORCEPS, Substantially Equivalent on 1996-01-24. Applicant: Olympus America, Inc..

Clearance details

Applicant: Olympus America, Inc.
Product code: Code FCL
Advisory panel: Gastroenterology, Urology
Date received: 1995-11-06
Decision date: 1996-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, 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.