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Jms Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002352JMS A.V. FISTULA NEEDLE SET ACCORDION TYPESeptember 6, 2001
K002394JMS APHERESIS NEEDLE SET ACCORDION TYPESeptember 5, 2001
K010410JMS APHERESIS NEEDLE WING EATER, MODEL 14G-18GJune 20, 2001
K010406JMS A.V. FISTULA NEEDLE SET WING EATER, MODEL 14G-18GJune 20, 2001
K000845MODIFICATION TO JMS A.V. FISTULA NEEDLE SETApril 10, 2000
K000843MODIFICATION TO JMS APHERESIS NEEDLEApril 10, 2000
K991904MODIFICATION OF JMS NEEDLES AND JMS SYRINGESAugust 31, 1999
K990510JMS APHERESIS NEEDLEAugust 30, 1999
K990470JMS A. V. FISTULA NEEDLE SETAugust 30, 1999
K983707JMS DIALYZER PRIMING SETJanuary 8, 1999
K974902JMS APHERESIS NEEDLEMarch 30, 1998
K970962JMS AV FISTULA NEEDLEAugust 7, 1997
K965027VENTED I.V. SETJune 24, 1997
K915174JMS APHERESIS NEEDLEMarch 2, 1993
K911199JMS AV FISTULA NEEDLESAugust 28, 1991
K895882JMS DIALYZER PRIMING SETFebruary 9, 1990
K880726JMS APHERESIS NEEDLEMarch 16, 1988
K880174JMS TRANSFUSION SETFebruary 16, 1988
K871965JMS NEEDLES AND JMS SYRINGESSeptember 4, 1987
K864747VARIOUS SYRINGES W/NEEDLES, W/OUT NEEDLES, NEEDLESDecember 29, 1986