FDA 510(k), K081791, E-Z CLEAN ELECTROSURGICAL ELECTRODE

FDA 510(k), K081791, E-Z CLEAN ELECTROSURGICAL ELECTRODE

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510(K) Number: K081791
Device Name: E-Z CLEAN ELECTROSURGICAL ELECTRODE
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 06/25/2008
Decision Date: 10/21/2008
Regulation Medical Specialty: General & Plastic Surgery
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