MODIFICATION TO RETINAL FUNCTION IMAGER (RFI)— 510(k) K080180
Substantially EquivalentOptical Imaging , Ltd.
FDA 510(k) clearance K080180 for MODIFICATION TO RETINAL FUNCTION IMAGER (RFI), Substantially Equivalent on 2008-06-11. Applicant: Optical Imaging , Ltd.. Device class: 2.
Clearance details
- Applicant
- Optical Imaging , Ltd.
- Product code
- Code HKI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1120
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code HKI
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