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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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