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FDA 510(k), K130752, DYNASENSE SYSTEM
FDA 510(k), K130752, DYNASENSE SYSTEM
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510(K) Number: K130752
Device Name: DYNASENSE SYSTEM
Manufacturer: CENTAURI MEDICAL, INC.
Device Classification Name: Monitor, Bed Patient
Regulation Number: 880.2400
Classification Product Code: KMI
Date Received: 03/19/2013
Decision Date: 08/15/2013
Regulation Medical Specialty: General Hospital
Device Name: DYNASENSE SYSTEM
Manufacturer: CENTAURI MEDICAL, INC.
Device Classification Name: Monitor, Bed Patient
Regulation Number: 880.2400
Classification Product Code: KMI
Date Received: 03/19/2013
Decision Date: 08/15/2013
Regulation Medical Specialty: General Hospital
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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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