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FDA 510(k), K200183, CS 9600
FDA 510(k), K200183, CS 9600
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510(K) Number: K200183
Device Name: CS 9600
Manufacturer: Trophy
Device Classification Name: x-ray, tomography, computed, dental
Regulation Number: 892.1750
Classification Product Code: OAS
Date Received: 01/24/2020
Decision Date: 03/13/2020
Regulation Medical Specialty: Radiology
Device Name: CS 9600
Manufacturer: Trophy
Device Classification Name: x-ray, tomography, computed, dental
Regulation Number: 892.1750
Classification Product Code: OAS
Date Received: 01/24/2020
Decision Date: 03/13/2020
Regulation Medical Specialty: Radiology
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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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