FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARTHORALIX 8500, MODELS 110-0199G1, 110-0199G2, 110-0199G3, 110-0199G4
K Number: K050255
·
Decision Mar 17, 2005
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
2
Review Days
42
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Basic Information
- Device Name
- ARTHORALIX 8500, MODELS 110-0199G1, 110-0199G2, 110-0199G3, 110-0199G4
- K Number
- K050255
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.1800
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Gendex Dental Systems
- Date Received
- February 3, 2005
- Decision Date
- March 17, 2005
- Product Code
- EHD
- 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 |
|---|---|---|---|
| EHD | Unit, X-Ray, Extraoral With Timer | FDA class 2 | Dental |
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Other Clearances by Gendex Dental Systems
| K Number | Device Name | ||
|---|---|---|---|
| K060178 | VIX WIN PRO | Mar 10, 2006 | Substantially Equivalent |