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FDA 510(k), K040687, ONEDOSE PATIENT DOSIMETRY SYSTEM
FDA 510(k), K040687, ONEDOSE PATIENT DOSIMETRY SYSTEM
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510(K) Number: K040687
Device Name: ONEDOSE PATIENT DOSIMETRY SYSTEM
Manufacturer: SICEL TECHNOLOGIES INC
Device Classification Name: accelerator, linear, medical
Regulation Number: 892.5050
Classification Product Code: IYE
Date Received: 03/16/2004
Decision Date: 06/25/2004
Regulation Medical Specialty: Radiology
Device Name: ONEDOSE PATIENT DOSIMETRY SYSTEM
Manufacturer: SICEL TECHNOLOGIES INC
Device Classification Name: accelerator, linear, medical
Regulation Number: 892.5050
Classification Product Code: IYE
Date Received: 03/16/2004
Decision Date: 06/25/2004
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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