DAUM BIOPSYNEEDLE— 510(k) K961185

Substantially Equivalent

Ferguson Medical

FDA 510(k) clearance K961185 for DAUM BIOPSYNEEDLE, Substantially Equivalent on 1996-04-30. Applicant: Ferguson Medical.

Clearance details

Applicant: Ferguson Medical
Product code: Code FCG
Advisory panel: Gastroenterology, Urology
Date received: 1996-03-26
Decision date: 1996-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chico, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FCG

product code FCG

Death: 13
Injury: 576
Malfunction: 1,966
Total: 2,555

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.