FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
ORTHO VLC; ORTHO VLC CAPSULE
K Number: K011521
·
Decision Aug 1, 2001
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
5
Review Days
76
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Basic Information
- Device Name
- ORTHO VLC; ORTHO VLC CAPSULE
- K Number
- K011521
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3750
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- First Scientific Limited
- Date Received
- May 17, 2001
- Decision Date
- August 1, 2001
- 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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