CARDIARC SPECT IMAGING DEVICE, MODEL CQ103-RV2— 510(k) K053062
Substantially EquivalentCardiarc , Ltd.
FDA 510(k) clearance K053062 for CARDIARC SPECT IMAGING DEVICE, MODEL CQ103-RV2, Substantially Equivalent on 2006-01-06. Applicant: Cardiarc , Ltd..
Clearance details
- Applicant
- Cardiarc , Ltd.
- Product code
- Code KPS
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.