VISTA DIGITAL OPTHALMOSCOPE— 510(k) K102412
Substantially EquivalentEyequick.Llc
FDA 510(k) clearance K102412 for VISTA DIGITAL OPTHALMOSCOPE, Substantially Equivalent on 2011-06-23. Applicant: Eyequick.Llc. Device class: 2.
Clearance details
- Applicant
- Eyequick.Llc
- 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
- El Paso,Tx, TX, US
Recent devices under product code HKI
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