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FDA 510(k), K181269, iCertainty
FDA 510(k), K181269, iCertainty
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510(K) Number: K181269
Device Name: iCertainty
Manufacturer: Rfpi
Device Classification Name: flowmeter, blood, cardiovascular
Regulation Number: 870.2100
Classification Product Code: DPW
Date Received: 05/14/2018
Decision Date: 12/14/2018
Regulation Medical Specialty: Cardiovascular
Device Name: iCertainty
Manufacturer: Rfpi
Device Classification Name: flowmeter, blood, cardiovascular
Regulation Number: 870.2100
Classification Product Code: DPW
Date Received: 05/14/2018
Decision Date: 12/14/2018
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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