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510(k) K881876

Device
DYNAMIC CRUCIATE TESTER
Applicant
DYONICS, INC.
510(k) number
K881876
Product code
LYH  
Decision
Substantially Equivalent (SESE)
Decision date
1988-11-17
Date received
1988-05-04
Regulation
890.1615
Classification name
Arthrometer
Medical specialty
Physical Medicine
Review panel
Neurology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
KENNETH E CARRIER
Address
160 Dascomb Rd. Andover MA US 01810 01810

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
K942059KT2000 KNEE LIGAMENT ARTHROMETERMedmetric Corp.1994-09-20
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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