DAUM NEUROCUT NEUROBIOPSYNEEDLE— 510(k) K990278

Substantially Equivalent

Daum Corp.

FDA 510(k) clearance K990278 for DAUM NEUROCUT NEUROBIOPSYNEEDLE, Substantially Equivalent on 1999-03-30. Applicant: Daum Corp..

Clearance details

Applicant: Daum Corp.
Product code: Code KNW
Advisory panel: Gastroenterology, Urology
Date received: 1999-01-28
Decision date: 1999-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

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.