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FDA 510(k), K172457, Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM
FDA 510(k), K172457, Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM
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510(K) Number: K172457
Device Name: Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM
Manufacturer: Deltex Medical Limited
Device Classification Name: flowmeter, blood, cardiovascular
Regulation Number: 870.2100
Classification Product Code: DPW
Date Received: 08/14/2017
Decision Date: 06/28/2018
Regulation Medical Specialty: Cardiovascular
Device Name: Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM
Manufacturer: Deltex Medical Limited
Device Classification Name: flowmeter, blood, cardiovascular
Regulation Number: 870.2100
Classification Product Code: DPW
Date Received: 08/14/2017
Decision Date: 06/28/2018
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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