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FDA 510(k), K134032, ULTHERA SYSTEM
FDA 510(k), K134032, ULTHERA SYSTEM
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510(K) Number: K134032
Device Name: ULTHERA SYSTEM
Manufacturer: ASHLEY FICKETT
Device Classification Name: Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption
Regulation Number: OHV
Classification Product Code: 12/31/2013
Date Received: 06/20/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ULTHERA SYSTEM
Manufacturer: ASHLEY FICKETT
Device Classification Name: Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption
Regulation Number: OHV
Classification Product Code: 12/31/2013
Date Received: 06/20/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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