FDA 510(k) Applications Submitted by OPTICAL IMAGING LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K080180 01/24/2008 MODIFICATION TO RETINAL FUNCTION IMAGER (RFI) OPTICAL IMAGING LTD.
K062416 08/17/2006 RETINAL FUNCTIONAL IMAGER (RFI) OPTICAL IMAGING LTD.


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