FDA 510(k), K190070, Sonopet iQ Ultrasonic Aspirator System
FDA 510(k), K190070, Sonopet iQ Ultrasonic Aspirator System
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510(K) Number: K190070
Device Name: Sonopet iQ Ultrasonic Aspirator System
Manufacturer: Stryker Corporation
Device Classification Name: instrument, ultrasonic surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 01/15/2019
Decision Date: 04/11/2019
Regulation Medical Specialty:
Device Name: Sonopet iQ Ultrasonic Aspirator System
Manufacturer: Stryker Corporation
Device Classification Name: instrument, ultrasonic surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 01/15/2019
Decision Date: 04/11/2019
Regulation Medical Specialty:
- 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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