FDA 510(k) Applications Submitted by ACCUIMAGE DIAGNOSTICS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K990241 01/25/1999 ACCUIMAGE, ACCUVIEW DIAGNOSTIC IMAGING, WORKSTATION W/ACCUSCORE, ACCUANALYZE, ACCUSCOPE, ACCUSHADE, ACCUVRT, AND ACCUMIP ACCUIMAGE DIAGNOSTICS CORP.
K012106 07/06/2001 ACCUIMAGE SMARTGATE UPGRADE ACCUIMAGE DIAGNOSTICS CORP.
K024149 12/16/2002 PRIMELUNG ACCUIMAGE DIAGNOSTICS CORP.


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