Digital Radiography CXDI-Elite, Digital Radiography E1— 510(k) K221620
Substantially EquivalentCanon, Inc.
FDA 510(k) clearance K221620 for Digital Radiography CXDI-Elite, Digital Radiography E1, Substantially Equivalent on 2022-06-14. Applicant: Canon, Inc.. Device class: 2.
Clearance details
- Applicant
- Canon, 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
- Special
- Location
- Kawasaki, JP
Recent devices under product code MQB
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