FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
MAJOR.REPAIR
K Number: K082153
·
Decision Nov 25, 2008
Classifications
1
FEI Numbers
167
Registration Numbers
167
Same Product Code
322
Applicant Total
3
Review Days
118
Basic Information
- Device Name
- MAJOR.REPAIR
- K Number
- K082153
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3760
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MAJOR PRODOTTI DENTARI S.P.A.
- Date Received
- July 30, 2008
- Decision Date
- November 25, 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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