FDA 510(k), K052852, SUPERDIMENSION/BRONCHUS PREMIUM

FDA 510(k), K052852, SUPERDIMENSION/BRONCHUS PREMIUM

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510(K) Number: K052852
Device Name: SUPERDIMENSION/BRONCHUS PREMIUM
Manufacturer:
Device Classification Name: System, X-Ray, Tomography, Computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 10/11/2005
Decision Date: 11/14/2005
Regulation Medical Specialty: Radiology
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