FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ALCON MULTI-PURPOSE SOLUTION
K Number: K071236
·
Decision Dec 12, 2007
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
119
Applicant Total
3
Review Days
223
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Basic Information
- Device Name
- ALCON MULTI-PURPOSE SOLUTION
- K Number
- K071236
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.5928
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Alcon, Inc.
- Date Received
- May 3, 2007
- Decision Date
- December 12, 2007
- Product Code
- LPN
- 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 |
|---|---|---|---|
| LPN | Accessories, Soft Lens Products | FDA class 2 | Ophthalmic |
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