FDA 510(k) Applications Submitted by JMS CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K010406 02/12/2001 JMS A.V. FISTULA NEEDLE SET WING EATER, MODEL 14G-18G JMS CO., LTD.
K010410 02/12/2001 JMS APHERESIS NEEDLE WING EATER, MODEL 14G-18G JMS CO., LTD.
K000843 03/15/2000 MODIFICATION TO JMS APHERESIS NEEDLE JMS CO., LTD.
K000845 03/15/2000 MODIFICATION TO JMS A.V. FISTULA NEEDLE SET JMS CO., LTD.
K991904 06/04/1999 MODIFICATION OF JMS NEEDLES AND JMS SYRINGES JMS CO., LTD.
K002352 08/02/2000 JMS A.V. FISTULA NEEDLE SET ACCORDION TYPE JMS CO., LTD.
K002394 08/07/2000 JMS APHERESIS NEEDLE SET ACCORDION TYPE JMS CO., LTD.
K970962 03/17/1997 JMS AV FISTULA NEEDLE JMS CO., LTD.
K974902 12/30/1997 JMS APHERESIS NEEDLE JMS CO., LTD.
K990470 02/16/1999 JMS A. V. FISTULA NEEDLE SET JMS CO., LTD.
K990510 02/18/1999 JMS APHERESIS NEEDLE JMS CO., LTD.
K983707 10/21/1998 JMS DIALYZER PRIMING SET JMS CO., LTD.
K965027 12/17/1996 VENTED I.V. SET JMS CO., LTD.


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