Fujimori Kogyo Co L T D Mie Facility

FDA Filings

This page includes the latest FDA filings for Fujimori Kogyo Co L T D Mie Facility. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3016571810
FEI Number3016571810
NameFUJIMORI KOGYO CO., LTD. MIE FACILITY
Owner & OperatorFUJIMORI KOGYO CO., LTD.
Contact Address1-23-7 NISHI-SHINJUKU, SHINJUKU-KU
TOKYO JP-13 Tokyo 1600023 JP
Official Correspondent
  • Yoshihiro Soya
  • 81-3-63812573-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3889-1, GITCHOBO, TAKINOHARA
NABARI CITY Mie, 518-0411 JP
Establishment TypeComplaint File Establishment per 21 CFR 820.198

FDA Filings

Device
Company
DeviceDate
FUJIMORI KOGYO CO., LTD. MIE FACILITY [FUJIMORI KOGYO CO., LTD.]
T-TAS 01 Total Thrombus Formation Analysis System Instrument2020-02-22
FUJIMORI KOGYO CO., LTD. MIE FACILITY [FUJIMORI KOGYO CO., LTD.]
PL Chip for T-TAS 012020-02-22
FUJIMORI KOGYO CO., LTD. MIE FACILITY [FUJIMORI KOGYO CO., LTD.]
PL Chip Reservoir Set for T-TAS 012020-02-22
FUJIMORI KOGYO CO., LTD. MIE FACILITY [FUJIMORI KOGYO CO., LTD.]
BAPA Tube for T-TAS 012020-02-22

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