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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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