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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cannula, Ophthalmic
510(k) Number K872151
Device Name OPHTHALMIC CANNULA
Applicant
Pharmacia, Inc.
1124 Kiefer Creek Meadows Dr.
St. Louis,  MO  63021
Applicant Contact DICK, PH.D.
Correspondent
Pharmacia, Inc.
1124 Kiefer Creek Meadows Dr.
St. Louis,  MO  63021
Correspondent Contact DICK, PH.D.
Regulation Number886.4350
Classification Product Code
HMX  
Date Received06/04/1987
Decision Date 06/19/1987
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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