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FDA 510(k), K153371, Sonicision Cordless Ultrasonic Dissection Device
FDA 510(k), K153371, Sonicision Cordless Ultrasonic Dissection Device
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510(K) Number: K153371
Device Name: Sonicision Cordless Ultrasonic Dissection Device
Manufacturer: COVIDIEN LLC
Device Classification Name: instrument, ultrasonic surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 11/23/2015
Decision Date: 03/28/2016
Regulation Medical Specialty:
Device Name: Sonicision Cordless Ultrasonic Dissection Device
Manufacturer: COVIDIEN LLC
Device Classification Name: instrument, ultrasonic surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 11/23/2015
Decision Date: 03/28/2016
Regulation Medical Specialty:
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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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