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FDA 510(k), K073262, BELLA
FDA 510(k), K073262, BELLA
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510(K) Number: K073262
Device Name: BELLA
Manufacturer: BEEKLEY CORP.
Device Classification Name: system, x-ray, mammographic
Regulation Number: 892.1710
Classification Product Code: IZH
Date Received: 11/20/2007
Decision Date: 03/26/2008
Regulation Medical Specialty: Radiology
Device Name: BELLA
Manufacturer: BEEKLEY CORP.
Device Classification Name: system, x-ray, mammographic
Regulation Number: 892.1710
Classification Product Code: IZH
Date Received: 11/20/2007
Decision Date: 03/26/2008
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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