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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lacrimal Stents And Intubation Sets
510(k) Number K962151
Device Name RYDER LACRIMAL INTUBATIONSET
Applicant
Ryder Intl. Corp.
1426 Curt Francis Rd.
Arab,  AL  35016
Applicant Contact DAN CLARK
Correspondent
Ryder Intl. Corp.
1426 Curt Francis Rd.
Arab,  AL  35016
Correspondent Contact DAN CLARK
Classification Product Code
OKS  
Date Received06/04/1996
Decision Date 09/18/1996
Decision Substantially Equivalent (SESE)
510k Review Panel Ophthalmic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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