FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
MAJOR.BASE 20
K Number: K081884
·
Decision Oct 8, 2008
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
3
Review Days
98
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Basic Information
- Device Name
- MAJOR.BASE 20
- K Number
- K081884
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 872.3760
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Major Prodotti Dentari S.P.A.
- Date Received
- July 2, 2008
- Decision Date
- October 8, 2008
- Product Code
- EBI
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- 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 |
|---|---|---|---|
| EBI | Resin, Denture, Relining, Repairing, Rebasing | FDA class 2 | Dental |
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