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FDA 510(k), K011056, ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD
FDA 510(k), K011056, ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD
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510(K) Number: K011056
Device Name: ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD
Manufacturer: THOMAS D NICKEL
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: QEW
Classification Product Code: 04/06/2001
Date Received: 10/24/2001
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD
Manufacturer: THOMAS D NICKEL
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: QEW
Classification Product Code: 04/06/2001
Date Received: 10/24/2001
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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