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FDA 510(k), K190269, PureLift
FDA 510(k), K190269, PureLift
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$149.00 USD
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$149.00 USD
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510(K) Number: K190269
Device Name: PureLift
Manufacturer: Xtreem Pulse, LLC
Device Classification Name: stimulator, transcutaneous electrical, aesthetic purposes
Regulation Number: 882.5890
Classification Product Code: NFO
Date Received: 02/08/2019
Decision Date: 08/28/2019
Regulation Medical Specialty: Neurology
Device Name: PureLift
Manufacturer: Xtreem Pulse, LLC
Device Classification Name: stimulator, transcutaneous electrical, aesthetic purposes
Regulation Number: 882.5890
Classification Product Code: NFO
Date Received: 02/08/2019
Decision Date: 08/28/2019
Regulation Medical Specialty: Neurology
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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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