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FDA 510(k), K990642, ECHOFLOW DOPPLER BLOOD VELOCITY METER
FDA 510(k), K990642, ECHOFLOW DOPPLER BLOOD VELOCITY METER
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510(K) Number: K990642
Device Name: ECHOFLOW DOPPLER BLOOD VELOCITY METER
Manufacturer: GEPRGE MYERS
Device Classification Name: Transducer, Ultrasonic
Regulation Number: JOP
Classification Product Code: 02/26/1999
Date Received: 09/16/1999
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: ECHOFLOW DOPPLER BLOOD VELOCITY METER
Manufacturer: GEPRGE MYERS
Device Classification Name: Transducer, Ultrasonic
Regulation Number: JOP
Classification Product Code: 02/26/1999
Date Received: 09/16/1999
Decision Date: Substantially Equivalent (SESE)
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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