FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GLASS IONOMER BASE
K Number: K882751
·
Decision Nov 29, 1988
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
76
Applicant Total
279
Review Days
147
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Basic Information
- Device Name
- GLASS IONOMER BASE
- K Number
- K882751
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3250
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Dentsply Intl.
- Date Received
- July 5, 1988
- Decision Date
- November 29, 1988
- Product Code
- EJK
- 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 |
|---|---|---|---|
| EJK | Liner, Cavity, Calcium Hydroxide | FDA class 2 | Dental |
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