FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
SAUFLON CLARITI 1 DAY WITH TINT (TORIC/MULTIFOCAL)
K Number: K133472
·
Decision Mar 4, 2014
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
485
Applicant Total
1
Review Days
112
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Basic Information
- Device Name
- SAUFLON CLARITI 1 DAY WITH TINT (TORIC/MULTIFOCAL)
- K Number
- K133472
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.5925
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Souflon Pharmaceuticals, Ltd.
- Date Received
- November 12, 2013
- Decision Date
- March 4, 2014
- Product Code
- LPL
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| LPL | Lenses, Soft Contact, Daily Wear | FDA class 2 | Ophthalmic |
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