XPLORER 2200 DIGITAL RADIOGRAPHIC SYSTEM— 510(k) K063039
Substantially EquivalentImaging Dynamics Company , Ltd.
FDA 510(k) clearance K063039 for XPLORER 2200 DIGITAL RADIOGRAPHIC SYSTEM, Substantially Equivalent on 2006-11-02. Applicant: Imaging Dynamics Company , Ltd..
Clearance details
- Applicant
- Imaging Dynamics Company , Ltd.
- Product code
- Code MQB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Calgary, Alberta, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.