FDA 510(k), K232809, Cross Vascular RF Generator and Footswitch (optional accessory)
FDA 510(k), K232809, Cross Vascular RF Generator and Footswitch (optional accessory)
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$149.00 USD
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$149.00 USD
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510(K) Number: K232809
Device Name: Cross Vascular RF Generator and Footswitch (optional accessory)
Manufacturer: Jennifer Willner
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: 09/12/2023
Date Received: 10/12/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Cross Vascular RF Generator and Footswitch (optional accessory)
Manufacturer: Jennifer Willner
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: 09/12/2023
Date Received: 10/12/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery