FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TAKE 1 ADVANCED RIGID TRAY
K Number: K092176
·
Decision Jan 28, 2010
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
399
Applicant Total
25
Review Days
191
Basic Information
- Device Name
- TAKE 1 ADVANCED RIGID TRAY
- K Number
- K092176
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3660
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- KERR CORPORATION
- Date Received
- July 21, 2009
- Decision Date
- January 28, 2010
- Product Code
- ELW
- 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 |
|---|---|---|---|
| ELW | Material, Impression | FDA class 2 | Dental |
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