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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name gauge, measuring
510(k) Number K874569
Device Name SUREDROP EYEDROP GUIDE
Applicant
SUREDROP, INC.
P.O. BOX 123
TIGER,  GA  30576
Applicant Contact WILLIAM SMITH
Correspondent
SUREDROP, INC.
P.O. BOX 123
TIGER,  GA  30576
Correspondent Contact WILLIAM SMITH
Regulation Number874.4420
Classification Product Code
JYJ  
Date Received11/05/1987
Decision Date 05/03/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
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