BAUER FLEXI-TEMNO BIOPSY NEEDLE— 510(k) K902320

Substantially Equivalent

Proact, Ltd.

FDA 510(k) clearance K902320 for BAUER FLEXI-TEMNO BIOPSY NEEDLE, Substantially Equivalent on 1990-10-01. Applicant: Proact, Ltd..

Clearance details

Applicant: Proact, Ltd.
Product code: Code FCG
Advisory panel: Gastroenterology, Urology
Date received: 1990-05-23
Decision date: 1990-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: State College, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FCG

product code FCG

Death: 13
Injury: 576
Malfunction: 1,966
Total: 2,555

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.