FDA 510(k)
FDA class 2
Substantially Equivalent
🇯🇵 Japan
Mammography Color Display DP-M3010
K Number: K143718
·
Decision Jan 22, 2015
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
134
Applicant Total
43
Review Days
24
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Basic Information
- Device Name
- Mammography Color Display DP-M3010
- K Number
- K143718
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Canon, Inc.
- Date Received
- December 29, 2014
- Decision Date
- January 22, 2015
- Product Code
- PGY
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PGY | Display, Diagnostic Radiology | FDA class 2 | Radiology |
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