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FDA 510(k), K103059, TROPHON
FDA 510(k), K103059, TROPHON
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510(K) Number: K103059
Device Name: TROPHON
Manufacturer: NANOSONICS LIMITED
Device Classification Name: high level disinfection reprocessing instrument for ultrasonic transducers, mist
Regulation Number: 892.1570
Classification Product Code: OUJ
Date Received: 10/15/2010
Decision Date: 02/24/2011
Regulation Medical Specialty: Radiology
Device Name: TROPHON
Manufacturer: NANOSONICS LIMITED
Device Classification Name: high level disinfection reprocessing instrument for ultrasonic transducers, mist
Regulation Number: 892.1570
Classification Product Code: OUJ
Date Received: 10/15/2010
Decision Date: 02/24/2011
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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