IMAX CEPH DIGITAL X-RAY SENSOR— 510(k) K062403
Substantially EquivalentOwandy
FDA 510(k) clearance K062403 for IMAX CEPH DIGITAL X-RAY SENSOR, Substantially Equivalent on 2006-11-14. Applicant: Owandy.
Clearance details
- Applicant
- Owandy
- Product code
- Code MUH
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ormond Beach, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.