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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name forceps, ophthalmic
510(k) Number K895434
Device Name ALCON FOLDING FORCEPS
Applicant
ALCON LABORATORIES
6201 SOUTH FREEWAY
R7-14
FORT WORTH,  TX  76134 -2099
Applicant Contact G WALKER
Correspondent
ALCON LABORATORIES
6201 SOUTH FREEWAY
R7-14
FORT WORTH,  TX  76134 -2099
Correspondent Contact G WALKER
Regulation Number886.4350
Classification Product Code
HNR  
Date Received09/08/1989
Decision Date 12/04/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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