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FDA 510(k), K062817, PTW DAVID IMRT QC VERIFICATION SYSTEM
FDA 510(k), K062817, PTW DAVID IMRT QC VERIFICATION SYSTEM
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$149.00 USD
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510(K) Number: K062817
Device Name: PTW DAVID IMRT QC VERIFICATION SYSTEM
Manufacturer: PTW-NEW YORK CORP.
Device Classification Name: accelerator, linear, medical
Regulation Number: 892.5050
Classification Product Code: IYE
Date Received: 09/20/2006
Decision Date: 11/22/2006
Regulation Medical Specialty: Radiology
Device Name: PTW DAVID IMRT QC VERIFICATION SYSTEM
Manufacturer: PTW-NEW YORK CORP.
Device Classification Name: accelerator, linear, medical
Regulation Number: 892.5050
Classification Product Code: IYE
Date Received: 09/20/2006
Decision Date: 11/22/2006
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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