BIOPSY FORCEPS— 510(k) K924106

Substantially Equivalent

United States Endoscopy Group, Inc.

FDA 510(k) clearance K924106 for BIOPSY FORCEPS, Substantially Equivalent on 1992-11-24. Applicant: United States Endoscopy Group, Inc..

Clearance details

Applicant: United States Endoscopy Group, Inc.
Product code: Code KNW
Advisory panel: Gastroenterology, Urology
Date received: 1992-08-13
Decision date: 1992-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, 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.