ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM


Device Classification Name

aberrometer, ophthalmic

510(k) Number K023249
Device Name ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM
Original Applicant
ALCON LABORATORIES, INC.
2501 discovery drive,suite 500
orlando, 
FL 
32826 -3714

Original Contact christy stevens
Regulation Number 886.1760
Classification Product Code
NCF  
Date Received 09/30/2002
Decision Date 10/18/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Ophthalmic

510k Review Panel

Ophthalmic

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls