NON-ELECTRIC BIOPSY FORCEPS— 510(k) K900015

Substantially Equivalent

Esco Precision, Inc.

FDA 510(k) clearance K900015 for NON-ELECTRIC BIOPSY FORCEPS, Substantially Equivalent on 1990-03-15. Applicant: Esco Precision, Inc..

Clearance details

Applicant: Esco Precision, Inc.
Product code: Code FCL
Advisory panel: Gastroenterology, Urology
Date received: 1990-01-02
Decision date: 1990-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stony Brook, 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.