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.. Device class: 2.
Clearance details
- Applicant
- Canon USA, Inc.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Success, NY, US
Recent devices under product code MQB
view allMore clearances from Canon USA, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.