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FDA 510(k), K010309, SONOPET MODEL UST-2001 ULTRASONIC SURGICAL ASPIRATOR
FDA 510(k), K010309, SONOPET MODEL UST-2001 ULTRASONIC SURGICAL ASPIRATOR
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510(K) Number: K010309
Device Name: SONOPET MODEL UST-2001 ULTRASONIC SURGICAL ASPIRATOR
Manufacturer: MUTOH AMERICA CO., LTD.
Device Classification Name: instrument, ultrasonic surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 02/01/2001
Decision Date: 04/18/2001
Regulation Medical Specialty:
Device Name: SONOPET MODEL UST-2001 ULTRASONIC SURGICAL ASPIRATOR
Manufacturer: MUTOH AMERICA CO., LTD.
Device Classification Name: instrument, ultrasonic surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 02/01/2001
Decision Date: 04/18/2001
Regulation Medical Specialty:
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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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