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510(k) K942059

Device
KT2000 KNEE LIGAMENT ARTHROMETER
Applicant
MEDMETRIC CORP.
510(k) number
K942059
Product code
LYH  
Decision
Substantially Equivalent (SESE)
Decision date
1994-09-20
Date received
1994-04-29
Regulation
890.1615
Classification name
Arthrometer
Medical specialty
Physical Medicine
Review panel
Neurology
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
K.R. WATKINS
Address
7542 Trade St. San Diego CA US 92121 92121

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LYH  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K943197KT1000/S KNEE LIGAMENT ARTHROMETERMedmetric Corp.1995-03-02
K881876DYNAMIC CRUCIATE TESTERDyonics, Inc.1988-11-17
K834462GENUCOMFar Orthopedics, Inc.1984-02-09
K812806KT-1000 DEVICEMedmetric Corp.1981-11-10

Legacy Summary#

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FDA Review#

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