BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910— 510(k) K012018

Substantially Equivalent

Acmi Corporation

FDA 510(k) clearance K012018 for BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910, Substantially Equivalent on 2002-07-16. Applicant: Acmi Corporation.

Clearance details

Applicant: Acmi Corporation
Product code: Code GEI
Advisory panel: General, Plastic Surgery
Date received: 2001-06-28
Decision date: 2002-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Southborough, MA, US

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Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

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.