MENICON PROGENT REMOVER— 510(k) K002140
Substantially EquivalentMenicon Co, Ltd.
FDA 510(k) clearance K002140 for MENICON PROGENT REMOVER, Substantially Equivalent on 2000-10-10. 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.