ROSE K LENS— 510(k) K945955
Substantially EquivalentRose K International , Ltd.
FDA 510(k) clearance K945955 for ROSE K LENS, Substantially Equivalent on 1995-02-07. Applicant: Rose K International , Ltd.. Device class: 2.
Clearance details
- Applicant
- Rose K International , Ltd.
- Product code
- Code HQD
- Device class
- Class 2
- Regulation
- 21 CFR 886.5916
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hamilton, NZ
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