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FDA 510(k), K173865, trophon2
FDA 510(k), K173865, trophon2
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$149.00 USD
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$149.00 USD
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510(K) Number: K173865
Device Name: trophon2
Manufacturer: Ruth Cremin
Device Classification Name: High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Mist
Regulation Number: OUJ
Classification Product Code: 12/20/2017
Date Received: 04/24/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: trophon2
Manufacturer: Ruth Cremin
Device Classification Name: High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Mist
Regulation Number: OUJ
Classification Product Code: 12/20/2017
Date Received: 04/24/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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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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