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FDA 510(k), K910007, SPRINGFUSOR 10R
FDA 510(k), K910007, SPRINGFUSOR 10R
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510(K) Number: K910007
Device Name: SPRINGFUSOR 10R
Manufacturer: DAVID CAPES
Device Classification Name: Pump, Infusion
Regulation Number: FRN
Classification Product Code: 01/02/1991
Date Received: 11/02/1993
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: SPRINGFUSOR 10R
Manufacturer: DAVID CAPES
Device Classification Name: Pump, Infusion
Regulation Number: FRN
Classification Product Code: 01/02/1991
Date Received: 11/02/1993
Decision Date: Substantially Equivalent (SESE)
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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