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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name arthrometer
510(k) Number K943197
Device Name KT1000/S KNEE LIGAMENT ARTHROMETER
Applicant
MEDMETRIC CORP.
7542 TRADE ST.
SAN DIEGO,  CA  92121 -2412
Applicant Contact K.R. WATKINS
Correspondent
MEDMETRIC CORP.
7542 TRADE ST.
SAN DIEGO,  CA  92121 -2412
Correspondent Contact K.R. WATKINS
Regulation Number890.1615
Classification Product Code
LYH  
Date Received07/05/1994
Decision Date 03/02/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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