The following data is part of a premarket notification filed by Digirad Corp. with the FDA for Cardius-1, -2, -3, And Cardius 1,2,3 Xpo Spect Imaging Systems, 2020tc Spect Imaging System.
| Device ID | K082368 |
| 510k Number | K082368 |
| Device Name: | CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM |
| Classification | System, Tomography, Computed, Emission |
| Applicant | DIGIRAD CORP. 13950 STOWE DRIVE Poway, CA 92064 -8803 |
| Contact | Joel Tuckey |
| Correspondent | Joel Tuckey DIGIRAD CORP. 13950 STOWE DRIVE Poway, CA 92064 -8803 |
| Product Code | KPS |
| CFR Regulation Number | 892.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-18 |
| Decision Date | 2008-09-12 |
| Summary: | summary |