FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KERATOR
K Number: K132144
·
Decision Mar 21, 2014
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
3
Review Days
253
Basic Information
- Device Name
- KERATOR
- K Number
- K132144
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- LK Consulting Group USA, Inc.
- Date Received
- July 11, 2013
- Decision Date
- March 21, 2014
- Product Code
- DZE
- 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 |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | FDA class 2 | Dental |
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