FDA 510(k), K133317, PENUMBRA SYSTEM / PENUMBRA SYSTEM MAX
FDA 510(k), K133317, PENUMBRA SYSTEM / PENUMBRA SYSTEM MAX
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$149.00 USD
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$149.00 USD
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510(K) Number: K133317
Device Name: PENUMBRA SYSTEM / PENUMBRA SYSTEM MAX
Manufacturer: PENUMBRA, INC.
Device Classification Name: catheter, thrombus retriever
Regulation Number: 870.1250
Classification Product Code: NRY
Date Received: 10/28/2013
Decision Date: 05/13/2014
Regulation Medical Specialty: Cardiovascular
Device Name: PENUMBRA SYSTEM / PENUMBRA SYSTEM MAX
Manufacturer: PENUMBRA, INC.
Device Classification Name: catheter, thrombus retriever
Regulation Number: 870.1250
Classification Product Code: NRY
Date Received: 10/28/2013
Decision Date: 05/13/2014
Regulation Medical Specialty: Cardiovascular