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FDA 510(k) Applications Submitted by MICHAEL DAYTON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140138
01/22/2014
HEARTNAVIGATOR RELEASE 2.0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K990227
01/25/1999
ULTRASHAPER KERATOME
LASERSIGHT TECHNOLOGIES, INC.
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