Identifiers
- 510(k) Number
- K002140 FDA 510(k)
- FDA Product Code
- MRC FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 886.5918 FDA 510(k)
- Regulation Number
- 886.5918 FDA 510(k)
- Advisory Committee
- Ophthalmic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Menicon Progent Remover by Menicon Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K002140 | Class II | Active |
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Manufacturer
- Manufacturer
- Menicon Co., Ltd.
- FDA Applicant
- Menicon Co, Ltd.
Sources (1)
- FDA 510(k) K002140 24 fields · synced Jun 19, 2026