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FDA 510(k), K052217, CRONO SUPER PID
FDA 510(k), K052217, CRONO SUPER PID
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510(K) Number: K052217
Device Name: CRONO SUPER PID
Manufacturer: CANE S.R.L.
Device Classification Name: pump, infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 08/15/2005
Decision Date: 09/13/2005
Regulation Medical Specialty: General Hospital
Device Name: CRONO SUPER PID
Manufacturer: CANE S.R.L.
Device Classification Name: pump, infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 08/15/2005
Decision Date: 09/13/2005
Regulation Medical Specialty: General Hospital
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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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