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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K863721
Device Name NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE
Applicant
Norfolk Medical Products, Inc.
7307 N. Ridgeway
Skokie,  IL  60076
Applicant Contact MICHAEL J DALTON
Correspondent
Norfolk Medical Products, Inc.
7307 N. Ridgeway
Skokie,  IL  60076
Correspondent Contact MICHAEL J DALTON
Date Received09/23/1986
Decision Date 10/14/1986
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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