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FDA 510(k) Applications Submitted by JAMES M ARGANDA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K161288
05/09/2016
LenSX Laser System
ALCON LABORATORIES, INC.
K173660
11/29/2017
LenSx Laser System
Alcon Laboratories, Inc.
K163551
12/19/2016
LenSx Laser System
Alcon Laboratories, Inc.
K952659
06/12/1995
TRONOMATE PATIENT CABLE & LEADWIRE SYSTEM
TRONOMED, INC.
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