FDA 510(k), K081379, MODIFICATION TO INREACH SYSTEM

FDA 510(k), K081379, MODIFICATION TO INREACH SYSTEM

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510(K) Number: K081379
Device Name: MODIFICATION TO INREACH SYSTEM
Manufacturer:
Device Classification Name: System, X-Ray, Tomography, Computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 05/16/2008
Decision Date: 06/11/2008
Regulation Medical Specialty: Radiology
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