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Cardius 1, 2 And 3 Xpo And 2020tc Spect Imaging Systems
FDA 510(k)Class II (US FDA 510(k))
510(k) K070542
Identifiers
- 510(k) Number
- K070542 FDA 510(k)
- FDA Product Code
- KPS FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 892.1200 FDA 510(k)
- Regulation Number
- 892.1200 FDA 510(k)
- Advisory Committee
- Radiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Cardius 1, 2 And 3 Xpo And 2020tc Spect Imaging Systems by Digirad Corp. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K070542 | Class II | Active |
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Manufacturer
- Manufacturer
- Digirad Corp.
Sources (1)
- FDA 510(k) K070542 24 fields · synced Jun 18, 2026