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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Holder, Needle; Orthopedic
510(k) Number K890167
Device Name HOLDER, NEEDLE
Applicant
DHASON BROTHERS, INC.
1705 MERRIMAK DR.
HYATTSVILLE,  MD  20783
Applicant Contact ROBERT DHASON
Correspondent
DHASON BROTHERS, INC.
1705 MERRIMAK DR.
HYATTSVILLE,  MD  20783
Correspondent Contact ROBERT DHASON
Regulation Number888.4540
Classification Product Code
HXK  
Date Received01/09/1989
Decision Date 02/03/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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