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FDA 510(k), K192833, Indigo Aspiration System
FDA 510(k), K192833, Indigo Aspiration System
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$149.00 USD
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510(K) Number: K192833
Device Name: Indigo Aspiration System
Manufacturer: Teri Nguyen
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: QEW
Classification Product Code: 10/02/2019
Date Received: 12/20/2019
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: Indigo Aspiration System
Manufacturer: Teri Nguyen
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: QEW
Classification Product Code: 10/02/2019
Date Received: 12/20/2019
Decision Date: Substantially Equivalent (SESE)
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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