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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070542
510(k) Type
Special
Applicant
Digirad Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2007
Days to Decision
25 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070542
510(k) Type
Special
Applicant
Digirad Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2007
Days to Decision
25 days
Submission Type
Summary