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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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