ELECTRO-SURGICAL DEVICES— 510(k) K771009

Substantially Equivalent

Deseret Pharmaceutical Co.

FDA 510(k) clearance K771009 for ELECTRO-SURGICAL DEVICES, Substantially Equivalent on 1977-07-13. Applicant: Deseret Pharmaceutical Co..

Clearance details

Applicant: Deseret Pharmaceutical Co.
Product code: Code GEI
Advisory panel: General, Plastic Surgery
Date received: 1977-06-03
Decision date: 1977-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sandy, UT, 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.