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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceWAVELIGHT EX500 LASER SYSTEM, ALLEGRO ANALYZER
Classification Nameexcimer laser system
Generic Nameexcimer laser system
Applicant
Alcon Laboratories, Inc.
6201 south freeway
fort worth, TX 76134-2099
PMA NumberP020050
Supplement NumberS011
Date Received01/18/2013
Decision Date04/12/2013
Product Code
LZS[ Registered Establishments with LZS ]
Advisory Committee Ophthalmic
Supplement Typereal-time process
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
APPROVAL TO INTRODUCE THE WAVENET¿ NETWORK SYSTEM TO FACILITATE DATA EXCHANGE BETWEEN FDA APPROVED/ CLEARED WAVELIGHT® REFRACTIVE/ THERAPEUTIC AND DIAGNOSTIC DEVICES VIA A NETWORK SERVER.
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