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FDA 510(k), K171022, Ablation Confirmation
FDA 510(k), K171022, Ablation Confirmation
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510(K) Number: K171022
Device Name: Ablation Confirmation
Manufacturer: NeuWave Medical, Inc.
Device Classification Name: system, x-ray, tomography, computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 04/05/2017
Decision Date: 05/09/2017
Regulation Medical Specialty: Radiology
Device Name: Ablation Confirmation
Manufacturer: NeuWave Medical, Inc.
Device Classification Name: system, x-ray, tomography, computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 04/05/2017
Decision Date: 05/09/2017
Regulation Medical Specialty: Radiology
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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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