AUTO-VAC BIOPSY NEEDLE— 510(k) K912892

Substantially Equivalent

Angiomed GmbH & Co. Medizintechnik KG

FDA 510(k) clearance K912892 for AUTO-VAC BIOPSY NEEDLE, Substantially Equivalent on 1992-02-07. Applicant: Angiomed GmbH & Co. Medizintechnik KG.

Clearance details

Applicant: Angiomed GmbH & Co. Medizintechnik KG
Product code: Code KNW
Advisory panel: Gastroenterology, Urology
Date received: 1991-07-01
Decision date: 1992-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Germany, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code KNW

product code KNW

Death: 9
Injury: 965
Malfunction: 10,444
Other: 3
Total: 11,421

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.