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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 K963501
Device Name HERRICK ULTIMATE PUNCTUM PLUG
Applicant
Lacrimedics, Inc.
190 N. Arrowhead Ave.,
Suite B
Rialto,  CA  92376
Applicant Contact ROBERT S HERRICK
Correspondent
Lacrimedics, Inc.
190 N. Arrowhead Ave.,
Suite B
Rialto,  CA  92376
Correspondent Contact ROBERT S HERRICK
Classification Product Code
LZU  
Date Received09/03/1996
Decision Date 04/14/1997
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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