FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EVOLVE
K Number: K033551
·
Decision Dec 16, 2003
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
32
Review Days
36
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Basic Information
- Device Name
- EVOLVE
- K Number
- K033551
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 872.3750
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Reliance Orthodontic Products, Inc.
- Date Received
- November 10, 2003
- Decision Date
- December 16, 2003
- Product Code
- DYH
- 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 |
|---|---|---|---|
| DYH | Adhesive, Bracket And Tooth Conditioner, Resin | FDA class 2 | Dental |
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