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FDA 510(k), K040066, SIREMOBILE C06
FDA 510(k), K040066, SIREMOBILE C06
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510(K) Number: K040066
Device Name: SIREMOBILE C06
Manufacturer: SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Classification Name: image-intensified fluoroscopic x-ray system, mobile
Regulation Number: 892.1650
Classification Product Code: OXO
Date Received: 01/13/2004
Decision Date: 02/12/2004
Regulation Medical Specialty: Radiology
Device Name: SIREMOBILE C06
Manufacturer: SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Classification Name: image-intensified fluoroscopic x-ray system, mobile
Regulation Number: 892.1650
Classification Product Code: OXO
Date Received: 01/13/2004
Decision Date: 02/12/2004
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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