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FDA 510(k), K052118, DOSE VERIFICATION SYSTEM
FDA 510(k), K052118, DOSE VERIFICATION SYSTEM
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510(K) Number: K052118
Device Name: DOSE VERIFICATION SYSTEM
Manufacturer: SICEL TECHNOLOGIES, INC.
Device Classification Name: system, radiation therapy, charged-particle, medical
Regulation Number: 892.5050
Classification Product Code: LHN
Date Received: 08/04/2005
Decision Date: 04/03/2006
Regulation Medical Specialty: Radiology
Device Name: DOSE VERIFICATION SYSTEM
Manufacturer: SICEL TECHNOLOGIES, INC.
Device Classification Name: system, radiation therapy, charged-particle, medical
Regulation Number: 892.5050
Classification Product Code: LHN
Date Received: 08/04/2005
Decision Date: 04/03/2006
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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