FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DENTIMAX DIGITAL X-RAY IMAGING SYSTEM SENSOR SIZE 1, 2, DENTIMAX USB CONTROL BOX
K Number: K092547
·
Decision Oct 30, 2009
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
1
Review Days
72
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Basic Information
- Device Name
- DENTIMAX DIGITAL X-RAY IMAGING SYSTEM SENSOR SIZE 1, 2, DENTIMAX USB CONTROL BOX
- K Number
- K092547
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.1800
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Dentimax
- Date Received
- August 19, 2009
- Decision Date
- October 30, 2009
- 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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