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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 K942059
Device Name KT2000 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 Received04/29/1994
Decision Date 09/20/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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