Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Ophthalmic Femtosecond Laser
510(k) Number K173660
Device Name LenSx Laser System
Applicant
Alcon Laboratories, Inc.
20511 Lake Forest Dr.
Lake Forest,  CA  92630
Applicant Contact James Arganda
Correspondent
Alcon Laboratories, Inc.
20511 Lake Forest Dr.
Lake Forest,  CA  92630
Correspondent Contact James Arganda
Regulation Number886.4390
Classification Product Code
OOE  
Subsequent Product Codes
HNO   HQC  
Date Received11/29/2017
Decision Date 03/27/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-