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FDA 510(k), K151319, Eko Electronic Stethoscope System
FDA 510(k), K151319, Eko Electronic Stethoscope System
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510(K) Number: K151319
Device Name: Eko Electronic Stethoscope System
Manufacturer: Eko Devices, Inc.
Device Classification Name: stethoscope, electronic
Regulation Number: 870.1875
Classification Product Code: DQD
Date Received: 05/18/2015
Decision Date: 08/28/2015
Regulation Medical Specialty: Cardiovascular
Device Name: Eko Electronic Stethoscope System
Manufacturer: Eko Devices, Inc.
Device Classification Name: stethoscope, electronic
Regulation Number: 870.1875
Classification Product Code: DQD
Date Received: 05/18/2015
Decision Date: 08/28/2015
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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