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FDA 510(k), K211798, Cleaner Plus Thrombectomy System
FDA 510(k), K211798, Cleaner Plus Thrombectomy System
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510(K) Number: K211798
Device Name: Cleaner Plus Thrombectomy System
Manufacturer: Ana Jimenez-Hughes
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: QEW
Classification Product Code: KXA
Date Received: 06/10/2021
Decision Date: 02/24/2022
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: Cleaner Plus Thrombectomy System
Manufacturer: Ana Jimenez-Hughes
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: QEW
Classification Product Code: KXA
Date Received: 06/10/2021
Decision Date: 02/24/2022
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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