CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK— 510(k) K881687

Substantially Equivalent

Cavitron Surgical Systems

FDA 510(k) clearance K881687 for CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK, Substantially Equivalent on 1988-06-20. Applicant: Cavitron Surgical Systems.

Clearance details

Applicant: Cavitron Surgical Systems
Product code: Code GEI
Advisory panel: General, Plastic Surgery
Date received: 1988-04-19
Decision date: 1988-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, 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.