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FDA 510(k), K901659, TITANIUM GREENFIELD(R) VENA CAVA FILTER W/HOOKS
FDA 510(k), K901659, TITANIUM GREENFIELD(R) VENA CAVA FILTER W/HOOKS
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510(K) Number: K901659
Device Name: TITANIUM GREENFIELD(R) VENA CAVA FILTER W/HOOKS
Manufacturer: BOSTON SCIENTIFIC CORP.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 04/10/1990
Decision Date: 11/08/1990
Regulation Medical Specialty: Cardiovascular
Device Name: TITANIUM GREENFIELD(R) VENA CAVA FILTER W/HOOKS
Manufacturer: BOSTON SCIENTIFIC CORP.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 04/10/1990
Decision Date: 11/08/1990
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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