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FDA 510(k), K032164, DIABETES DATA MANAGEMENT SYSTEM (DDMS), MODEL 7333
FDA 510(k), K032164, DIABETES DATA MANAGEMENT SYSTEM (DDMS), MODEL 7333
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510(K) Number: K032164
Device Name: DIABETES DATA MANAGEMENT SYSTEM (DDMS), MODEL 7333
Manufacturer: MEDTRONIC MINIMED
Device Classification Name: pump, infusion, insulin
Regulation Number: 880.5725
Classification Product Code: LZG
Date Received: 07/15/2003
Decision Date: 10/23/2003
Regulation Medical Specialty: General Hospital
Device Name: DIABETES DATA MANAGEMENT SYSTEM (DDMS), MODEL 7333
Manufacturer: MEDTRONIC MINIMED
Device Classification Name: pump, infusion, insulin
Regulation Number: 880.5725
Classification Product Code: LZG
Date Received: 07/15/2003
Decision Date: 10/23/2003
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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