BARD MONOPTY DISPOSABLE CORE BIOPSY INSTRUMENT— 510(k) K910190

Unknown

C.R. Bard, Inc.

FDA 510(k) clearance K910190 for BARD MONOPTY DISPOSABLE CORE BIOPSY INSTRUMENT, Unknown on 1991-08-16. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code KNW
Advisory panel: Gastroenterology, Urology
Date received: 1991-01-16
Decision date: 1991-08-16
Decision: Unknown
Clearance type: Traditional
Location: Covington, GA, US

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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.