Last synced on 25 January 2026 at 3:41 am

ACCUIMAGE, ACCUVIEW DIAGNOSTIC IMAGING, WORKSTATION W/ACCUSCORE, ACCUANALYZE, ACCUSCOPE, ACCUSHADE, ACCUVRT, AND ACCUMIP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990241
510(k) Type
Traditional
Applicant
Accuimage Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1999
Days to Decision
241 days
Submission Type
Summary

ACCUIMAGE, ACCUVIEW DIAGNOSTIC IMAGING, WORKSTATION W/ACCUSCORE, ACCUANALYZE, ACCUSCOPE, ACCUSHADE, ACCUVRT, AND ACCUMIP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990241
510(k) Type
Traditional
Applicant
Accuimage Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1999
Days to Decision
241 days
Submission Type
Summary