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FDA 510(k), K022238, MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626
FDA 510(k), K022238, MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626
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510(K) Number: K022238
Device Name: MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: instruments, surgical, cardiovascular
Regulation Number: 870.4500
Classification Product Code: DWS
Date Received: 07/11/2002
Decision Date: 10/09/2002
Regulation Medical Specialty: Cardiovascular
Device Name: MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: instruments, surgical, cardiovascular
Regulation Number: 870.4500
Classification Product Code: DWS
Date Received: 07/11/2002
Decision Date: 10/09/2002
Regulation Medical Specialty: Cardiovascular
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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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