FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENS
K Number: K122273
·
Decision Jan 2, 2013
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
32
Applicant Total
17
Review Days
156
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Basic Information
- Device Name
- MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENS
- K Number
- K122273
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 886.5918
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Menicon Co, Ltd.
- Date Received
- July 30, 2012
- Decision Date
- January 2, 2013
- Product Code
- MRC
- 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 |
|---|---|---|---|
| MRC | Products, Contact Lens Care, Rigid Gas Permeable | FDA class 2 | Ophthalmic |
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| K102895 | ONE DAY FLAT PACK | Apr 28, 2011 | Substantially Equivalent |
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| K082855 | MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES | Mar 9, 2010 | Substantially Equivalent |