Digirad Corp. · Class II · Cleared Mar 23, 2007
| K-number | K070542 |
| Device name | CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS |
| Applicant | Digirad Corp. |
| Product code | KPS |
| Device class | Class II |
| Decision date | Mar 23, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 892.1200 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov