FDA 510(k), K092365, INREACH SYSTEM, MODEL AAS00161-02

FDA 510(k), K092365, INREACH SYSTEM, MODEL AAS00161-02

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510(K) Number: K092365
Device Name: INREACH SYSTEM, MODEL AAS00161-02
Manufacturer:
Device Classification Name: System, X-Ray, Tomography, Computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 08/05/2009
Decision Date: 09/04/2009
Regulation Medical Specialty: Radiology
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