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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Probe, Test, Heart-Valve
510(k) Number K890165
Device Name FORCEPS-ORTHOPEDIC
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 Number870.4500
Classification Product Code
LXN  
Date Received01/09/1989
Decision Date 02/13/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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