Medicor USA , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K861994MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEMJuly 18, 1986
K861995MODEL RS-3 RADIOGRAPHIC STANDJune 19, 1986
K860025MODEL MS-325 RADIOGRAPHIC X-RAY GENERATORMay 7, 1986
K850761MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY CSeptember 19, 1985
K851358MODEL BION 2/TYPE 90 ROOM IONIZERJuly 1, 1985
K851094MODEL BION 1/TYPE 1084T CAR IONIZERJune 19, 1985
K843335FLOOR MOUNTED X-RAY TUBESTANDNovember 27, 1984
K840227UROLIX-3 UROLOGICAL TABLEMarch 23, 1984
K840225C-ARM CEILING CRANE FT-2March 22, 1984
K840226MOTOR TILTED EXAM. TABLE UV-56March 16, 1984
K823695CPM METABOLIC MONITORJanuary 14, 1983
K791287MEDICOR QUALITY CONTROL BUFFERAugust 16, 1979
K790803SYRINGE TONOMETERJune 28, 1979
K781417PRECISION GAS MIXERSeptember 20, 1978