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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Plug, Punctum
510(k) Number K896175
Device Name HERRICK LACRIMAL PLUG TM.
Applicant
Lacrimedics, Inc.
9008 Newby St.
Rosemead,  CA  91770
Applicant Contact ROBERT S HERRICK,II
Correspondent
Lacrimedics, Inc.
9008 Newby St.
Rosemead,  CA  91770
Correspondent Contact ROBERT S HERRICK,II
Classification Product Code
LZU  
Date Received10/25/1989
Decision Date 01/22/1990
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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