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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 K863991
Device Name THORTON TITANIUM NEEDLEHOLDERS(NO,W CATCH & STAND
Applicant
KEELER INSTRUMENTS, INC.
456 PKWY.
BROOMALL,  PA  19008
Applicant Contact VAN ARSDALE
Correspondent
KEELER INSTRUMENTS, INC.
456 PKWY.
BROOMALL,  PA  19008
Correspondent Contact VAN ARSDALE
Regulation Number886.4350
Classification Product Code
HNR  
Date Received10/14/1986
Decision Date 10/31/1986
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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