DeviceClearance

CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM— 510(k) K082368

Substantially Equivalent

Digirad Corp.

FDA 510(k) clearance K082368 for CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM, Substantially Equivalent on 2008-09-12. Applicant: Digirad Corp..

Clearance details

Applicant
Digirad Corp.
Product code
Code KPS
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Poway, CA, US
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