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FDA 510(k) Applications Submitted by SANDRA BROWN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070534
02/26/2007
MODIFICATION TO: OCU-FILM TIP COVER
REICHERT, INC.
K061330
05/12/2006
PSL PORTABLE SLIT LAMP
REICHERT, INC.
K081756
06/20/2008
OCULAR RESPONSE ANALYZER
REICHERT INC.
K071839
07/05/2007
SOCT COPERNICUS, MODEL 15205
REICHERT, INC.
K063750
12/19/2006
XCEL 255 SLIT LAMP
REICHERT INC.
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