FDA 510(k)
FDA class 2
Substantially Equivalent
🇯🇵 Japan
Menicon Saline Rinse Solution
K Number: K151768
·
Decision Aug 28, 2015
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
119
Applicant Total
17
Review Days
59
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Basic Information
- Device Name
- Menicon Saline Rinse Solution
- K Number
- K151768
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.5928
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Menicon Co, Ltd.
- Date Received
- June 30, 2015
- Decision Date
- August 28, 2015
- 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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