COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4— 510(k) K082051

Substantially Equivalent

Cosman Medical, Inc.

FDA 510(k) clearance K082051 for COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4, Substantially Equivalent on 2008-10-16. Applicant: Cosman Medical, Inc..

Clearance details

Applicant: Cosman Medical, Inc.
Product code: Code GXD
Advisory panel: Neurology
Date received: 2008-07-18
Decision date: 2008-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, MA, US

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Adverse events under product code GXD

product code GXD

Injury: 228
Total: 228

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.