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FDA 510(k), K102511, MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT
FDA 510(k), K102511, MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT
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510(K) Number: K102511
Device Name: MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 09/01/2010
Decision Date: 08/24/2011
Regulation Medical Specialty: Cardiovascular
Device Name: MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 09/01/2010
Decision Date: 08/24/2011
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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