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FDA 510(k), K112692, IDENTIFY
FDA 510(k), K112692, IDENTIFY
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510(K) Number: K112692
Device Name: IDENTIFY
Manufacturer: HUMEDIQ GMBH
Device Classification Name: accelerator, linear, medical
Regulation Number: 892.5050
Classification Product Code: IYE
Date Received: 09/15/2011
Decision Date: 08/03/2012
Regulation Medical Specialty: Radiology
Device Name: IDENTIFY
Manufacturer: HUMEDIQ GMBH
Device Classification Name: accelerator, linear, medical
Regulation Number: 892.5050
Classification Product Code: IYE
Date Received: 09/15/2011
Decision Date: 08/03/2012
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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