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FDA 510(k), K150657, Phoenix XL Dialysate Meter
FDA 510(k), K150657, Phoenix XL Dialysate Meter
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510(K) Number: K150657
Device Name: Phoenix XL Dialysate Meter
Manufacturer: Jamie Louie
Device Classification Name: Meter, Conductivity, Non-Remote
Regulation Number: FIZ
Classification Product Code: KXA
Date Received: 03/13/2015
Decision Date: 09/21/2015
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: Phoenix XL Dialysate Meter
Manufacturer: Jamie Louie
Device Classification Name: Meter, Conductivity, Non-Remote
Regulation Number: FIZ
Classification Product Code: KXA
Date Received: 03/13/2015
Decision Date: 09/21/2015
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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