FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LIGHT CURE DENTIN AND LINER BASE PRODUCT LINE
K Number: K921408
·
Decision Nov 24, 1992
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
76
Applicant Total
103
Review Days
245
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Basic Information
- Device Name
- LIGHT CURE DENTIN AND LINER BASE PRODUCT LINE
- K Number
- K921408
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3250
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Ultradent Products, Inc.
- Date Received
- March 24, 1992
- Decision Date
- November 24, 1992
- 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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