FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
K Clear
K Number: K220726
·
Decision Mar 16, 2022
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
143
Applicant Total
1
Review Days
2
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Basic Information
- Device Name
- K Clear
- K Number
- K220726
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.5470
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Kline Europe GmbH
- Date Received
- March 14, 2022
- Decision Date
- March 16, 2022
- Product Code
- NXC
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| NXC | Aligner, Sequential | FDA class 2 | Dental |
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