FDA 510(k), K072053, SMARTBLOCK PAIN PUMP
FDA 510(k), K072053, SMARTBLOCK PAIN PUMP
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510(K) Number: K072053
Device Name: SMARTBLOCK PAIN PUMP
Manufacturer: MEDICAL FLOW SYSTEMS LTD
Device Classification Name: pump, infusion, elastomeric
Regulation Number: 880.5725
Classification Product Code: MEB
Date Received: 07/26/2007
Decision Date: 11/06/2007
Regulation Medical Specialty: General Hospital
Device Name: SMARTBLOCK PAIN PUMP
Manufacturer: MEDICAL FLOW SYSTEMS LTD
Device Classification Name: pump, infusion, elastomeric
Regulation Number: 880.5725
Classification Product Code: MEB
Date Received: 07/26/2007
Decision Date: 11/06/2007
Regulation Medical Specialty: General Hospital
- 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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