FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DXS DIGITAL X-RAY SYSTEM
K Number: K013271
·
Decision Dec 13, 2001
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
1
Review Days
73
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Basic Information
- Device Name
- DXS DIGITAL X-RAY SYSTEM
- K Number
- K013271
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.1800
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Douglas C. Yoon, Dds
- Date Received
- October 1, 2001
- Decision Date
- December 13, 2001
- Product Code
- MUH
- Advisory Committee
- Dental
- 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 |
|---|---|---|---|
| MUH | System, X-Ray, Extraoral Source, Digital | FDA class 2 | Dental |
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