FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
GINGI CURETTAGE DIAMOND POINTS
K Number: K832856
·
Decision Oct 4, 1983
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
20
Applicant Total
59
Review Days
42
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Basic Information
- Device Name
- GINGI CURETTAGE DIAMOND POINTS
- K Number
- K832856
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4535
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Shofu Dental Corp.
- Date Received
- August 23, 1983
- Decision Date
- October 4, 1983
- Product Code
- DZP
- 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 |
|---|---|---|---|
| DZP | Instrument, Diamond, Dental | FDA class 1 | Dental |
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