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FDA 510(k), K121700, ULTHERA SYSTEM
FDA 510(k), K121700, ULTHERA SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K121700
Device Name: ULTHERA SYSTEM
Manufacturer: ULTHERA, INC.
Device Classification Name: Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption
Regulation Number: 878.4590
Classification Product Code: OHV
Date Received: 06/07/2012
Decision Date: 10/02/2012
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ULTHERA SYSTEM
Manufacturer: ULTHERA, INC.
Device Classification Name: Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption
Regulation Number: 878.4590
Classification Product Code: OHV
Date Received: 06/07/2012
Decision Date: 10/02/2012
Regulation Medical Specialty: General & Plastic Surgery
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