FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇷 Greece
Bright Temporary C&B
K Number: K192830
·
Decision Sep 2, 2020
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
3
Review Days
336
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Basic Information
- Device Name
- Bright Temporary C&B
- K Number
- K192830
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3770
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Dmp Dental Industry S.A.
- Date Received
- October 2, 2019
- Decision Date
- September 2, 2020
- Product Code
- EBG
- 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 |
|---|---|---|---|
| EBG | Crown And Bridge, Temporary, Resin | FDA class 2 | Dental |
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