FDA 510(k) Applications Submitted by CHARLINE GAUTHIER

FDA 510(k) Number Submission Date Device Name Applicant
K060372 02/13/2006 INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3 INTRA LASE CORP.
K001211 04/14/2000 MODIFICATION TO INTRALASE 600C LASER KERATOME INTRALASE CORP.
K031960 06/25/2003 INTRALASE FS LASER INTRALASE CORP.
K041893 07/13/2004 INTRALASE FS LASER INTRALASE CORP.
K002890 09/15/2000 INTRALASE 600C LASER KERATOME INTRALASE CORP.
K993153 09/21/1999 INTRALASE 600C LASER KERATOME INTRALASE CORP.
K013941 11/29/2001 PULSION FS LASER KERATOME INTRALASE CORP.


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