← Back to catalogue
Microkeratome, Model Mk-2000
FDA 510(k)Class I (US FDA 510(k))
510(k) K990900
by Nidek, Inc.
Identifiers
- 510(k) Number
- K990900 FDA 510(k)
- FDA Product Code
- HNO FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 886.4370 FDA 510(k)
- Regulation Number
- 886.4370 FDA 510(k)
- Advisory Committee
- Ophthalmic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Microkeratome, Model Mk-2000 by Nidek, Inc. — Class I — 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 | K990900 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Nidek, Inc.
Sources (1)
- FDA 510(k) K990900 24 fields · synced Jun 19, 2026