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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
Applicant Contact K.R. WATKINS
Correspondent
Medmetric Corp.
7542 Trade St.
San Diego,  CA  92121
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
Predetermined Change
Control Plan Authorized		 No
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