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FDA 510(k), K143310, MoisturemeterD
FDA 510(k), K143310, MoisturemeterD
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510(K) Number: K143310
Device Name: MoisturemeterD
Manufacturer: DELFIN TECHNOLOGIES LTD.
Device Classification Name: monitor, extracellular fluid, lymphedema, extremity
Regulation Number: 870.2770
Classification Product Code: OBH
Date Received: 11/18/2014
Decision Date: 11/19/2015
Regulation Medical Specialty: Cardiovascular
Device Name: MoisturemeterD
Manufacturer: DELFIN TECHNOLOGIES LTD.
Device Classification Name: monitor, extracellular fluid, lymphedema, extremity
Regulation Number: 870.2770
Classification Product Code: OBH
Date Received: 11/18/2014
Decision Date: 11/19/2015
Regulation Medical Specialty: Cardiovascular
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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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