MODIFICATION TO RETINAL FUNCTION IMAGER (RFI)— 510(k) K080180

Substantially Equivalent

Optical Imaging , Ltd.

FDA 510(k) clearance K080180 for MODIFICATION TO RETINAL FUNCTION IMAGER (RFI), Substantially Equivalent on 2008-06-11. Applicant: Optical Imaging , Ltd..

Clearance details

Applicant: Optical Imaging , Ltd.
Product code: Code HKI
Advisory panel: Ophthalmic
Date received: 2008-01-24
Decision date: 2008-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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