FDA 510(k), K062315, SUPERDIMENSION/BRONCHUS PREMIUM 2

FDA 510(k), K062315, SUPERDIMENSION/BRONCHUS PREMIUM 2

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510(K) Number: K062315
Device Name: SUPERDIMENSION/BRONCHUS PREMIUM 2
Manufacturer:
Device Classification Name: System, X-Ray, Tomography, Computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 08/09/2006
Decision Date: 09/08/2006
Regulation Medical Specialty: Radiology
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