FDA 510(k), K141122, HARMONIC SCALLOP BLADE, GENERATOR G11
FDA 510(k), K141122, HARMONIC SCALLOP BLADE, GENERATOR G11
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510(K) Number: K141122
Device Name: HARMONIC SCALLOP BLADE, GENERATOR G11
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 04/30/2014
Decision Date: 09/15/2014
Regulation Medical Specialty: General & Plastic Surgery
Device Name: HARMONIC SCALLOP BLADE, GENERATOR G11
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 04/30/2014
Decision Date: 09/15/2014
Regulation Medical Specialty: General & Plastic Surgery