FDA 510(k), K061035, TIGERVIEW PROFESSIONAL
FDA 510(k), K061035, TIGERVIEW PROFESSIONAL
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$149.00 USD
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510(K) Number: K061035
Device Name: TIGERVIEW PROFESSIONAL
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 04/14/2006
Decision Date: 06/05/2006
Regulation Medical Specialty: Radiology
Device Name: TIGERVIEW PROFESSIONAL
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 04/14/2006
Decision Date: 06/05/2006
Regulation Medical Specialty: Radiology