CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G
FDA 510(k) clearance K031447 · decided 2003-05-21
Clearance details
- K-number
- K031447
- Device name
- CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G
- Applicant
- Canon, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2003-05-07
- Decision date
- 2003-05-21
- Days to decision
- 14 days
- Clearance type
- Traditional
- Product code
- MQB
- Device class
- 2
- Regulation number
- 892.1680
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Lake Success, NY, US
- Third-party review
- Yes
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Canon
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.