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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lens, Contact (Polymethylmethacrylate)
510(k) Number K853728
Device Name KESTREL CONTACT LENS STORAGE CASE(NORYL)
Applicant
RYDER INTL. CORP.
100 CURT FRANCIS RD.
POST OFFICE BOX 564
ARAB,  AL  35016
Applicant Contact ANTHONY J MORAVEC
Correspondent
RYDER INTL. CORP.
100 CURT FRANCIS RD.
POST OFFICE BOX 564
ARAB,  AL  35016
Correspondent Contact ANTHONY J MORAVEC
Classification Product Code
HPX  
Date Received09/06/1985
Decision Date 12/13/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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