FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PALLADIUS-V AND PALLADIUS-AG SEMI-PRECIOUS ALLOY
K Number: K902863
·
Decision Oct 24, 1990
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
626
Applicant Total
36
Review Days
118
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Basic Information
- Device Name
- PALLADIUS-V AND PALLADIUS-AG SEMI-PRECIOUS ALLOY
- K Number
- K902863
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3060
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Vident
- Date Received
- June 28, 1990
- Decision Date
- October 24, 1990
- Product Code
- EJT
- 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 |
|---|---|---|---|
| EJT | Alloy, Gold-Based Noble Metal | FDA class 2 | Dental |
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