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FDA 510(k) Applications Submitted by JASON K LYON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090728
03/19/2009
HYPERGLIDE OCCLUSION BALLOON SYSTEM
EV3 INC.
K032412
08/05/2003
RE-USEABLE MICROSTAAR INJECTOR, MSI-S
STAAR SURGICAL CO.
K093554
11/17/2009
RETROFLEX DILATOR KIT
EDWARDS LIFESCIENCES, LLC.
K093877
12/16/2009
RETROFLEX 3 INTRODUCER SHEATH SET, MODELS 9120S23 AND 9120S26
EDWARDS LIFESCIENCES, LLC.
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