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FDA 510(k), K112930, MOBILE MIM
FDA 510(k), K112930, MOBILE MIM
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$149.00 USD
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$149.00 USD
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510(K) Number: K112930
Device Name: MOBILE MIM
Manufacturer: MIM SOFTWARE INC.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 10/03/2011
Decision Date: 12/02/2011
Regulation Medical Specialty: Radiology
Device Name: MOBILE MIM
Manufacturer: MIM SOFTWARE INC.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 10/03/2011
Decision Date: 12/02/2011
Regulation Medical Specialty: Radiology
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