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FDA 510(k), K161506, Penumbra Aspiration System
FDA 510(k), K161506, Penumbra Aspiration System
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$149.00 USD
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510(K) Number: K161506
Device Name: Penumbra Aspiration System
Manufacturer: Penumbra, Inc.
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: 870.5150
Classification Product Code: QEW
Date Received: 06/01/2016
Decision Date: 09/26/2016
Regulation Medical Specialty: Cardiovascular
Device Name: Penumbra Aspiration System
Manufacturer: Penumbra, Inc.
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: 870.5150
Classification Product Code: QEW
Date Received: 06/01/2016
Decision Date: 09/26/2016
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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