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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Anesthesia Conduction Kit
510(k) Number K895955
Device Name LOPER CELIAC PLEXUS BLOCK CATHETER KIT
Applicant
Opticon Medical, Inc.
806 Brian Court
Gurnee,  IL  60031
Applicant Contact JANE PATRICK
Correspondent
Opticon Medical, Inc.
806 Brian Court
Gurnee,  IL  60031
Correspondent Contact JANE PATRICK
Regulation Number868.5140
Classification Product Code
CAZ  
Date Received10/11/1989
Decision Date 02/22/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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