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Medmetric Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K943197KT1000/S KNEE LIGAMENT ARTHROMETERMarch 2, 1995
K942059KT2000 KNEE LIGAMENT ARTHROMETERSeptember 20, 1994
K904823FLEXERCYCLEJanuary 30, 1991
K904898TORQUE FRAME QTF1000November 28, 1990
K854254TENSION-ISOMETERNovember 15, 1985
K812806KT-1000 DEVICENovember 10, 1981
K812713DRAWER TESTNovember 5, 1981
K801572SURG-ASSISTAugust 4, 1980