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FDA 510(k), K073057, PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040
FDA 510(k), K073057, PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040
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510(K) Number: K073057
Device Name: PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040
Manufacturer: PEAK SURGICAL, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 10/30/2007
Decision Date: 07/22/2008
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040
Manufacturer: PEAK SURGICAL, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 10/30/2007
Decision Date: 07/22/2008
Regulation Medical Specialty: General & Plastic Surgery
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