FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
KETTOSIL AND SILGINAT
K Number: K082157
·
Decision Aug 6, 2008
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
13
Review Days
6
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Basic Information
- Device Name
- KETTOSIL AND SILGINAT
- K Number
- K082157
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3660
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Kettenbach GmbH & Co. KG
- Date Received
- July 31, 2008
- Decision Date
- August 6, 2008
- Product Code
- ELW
- 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 |
|---|---|---|---|
| ELW | Material, Impression | FDA class 2 | Dental |
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