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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Case, Contact Lens
510(k) Number K870164
Device Name SUMMIT OPTICS SOFT CONTACT LENS CASE
Applicant
Dayton Mfg. Co.
P.O. Box 271504
Tampa,  FL  33624
Applicant Contact MICHAEL P DAYTON,MA
Correspondent
Dayton Mfg. Co.
P.O. Box 271504
Tampa,  FL  33624
Correspondent Contact MICHAEL P DAYTON,MA
Regulation Number886.5928
Classification Product Code
LRX  
Date Received01/14/1987
Decision Date 02/10/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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