AUTOMATED CORE BIOPSY DEVICE— 510(k) K994272

Substantially Equivalent

Promex, Inc.

FDA 510(k) clearance K994272 for AUTOMATED CORE BIOPSY DEVICE, Substantially Equivalent on 2000-01-07. Applicant: Promex, Inc..

Clearance details

Applicant: Promex, Inc.
Product code: Code KNW
Advisory panel: Gastroenterology, Urology
Date received: 1999-12-20
Decision date: 2000-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin, IN, 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.