MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES— 510(k) K082855
Substantially EquivalentMenicon Co, Ltd.
FDA 510(k) clearance K082855 for MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES, Substantially Equivalent on 2010-03-09. Applicant: Menicon Co, Ltd.. Device class: 2.
Clearance details
- Applicant
- Menicon Co, Ltd.
- Product code
- Code MRC
- Device class
- Class 2
- Regulation
- 21 CFR 886.5918
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.