Last synced on 25 January 2026 at 3:41 am

CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082368
510(k) Type
Special
Applicant
Digirad Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
25 days
Submission Type
Summary

CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082368
510(k) Type
Special
Applicant
Digirad Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
25 days
Submission Type
Summary