CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G— 510(k) K023750
Substantially EquivalentCanon USA, Inc.
FDA 510(k) clearance K023750 for CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G, Substantially Equivalent on 2002-11-22. Applicant: Canon USA, Inc..
Clearance details
- Applicant
- Canon USA, Inc.
- Product code
- Code MQB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Success, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.