Hitachi High Technologies Corp Omuta Center

FDA Filings

This page includes the latest FDA filings for Hitachi High Technologies Corp Omuta Center. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014840402
FEI Number3014840402
NameHitachi High-Technologies Corp., Omuta Center
Owner & OperatorHITACHI HIGH-TECH CORP.
Contact Address1-17-1 Toranomon, --
Minato-ku JP-13 Tokyo 105-6409 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1892-1 Tegama
Omuta-shi, Fukuoka, 836-0004 JP
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Hitachi High-Technologies Corp., Omuta Center [HITACHI HIGH-TECH CORP.]
Clinical Laboratory Automation System (CLAS)2014-11-27
Hitachi High-Technologies Corp., Omuta Center [HITACHI HIGH-TECH CORP.]
cobas 8100 automated workflow series2014-11-24
Hitachi High-Technologies Corp., Omuta Center [HITACHI HIGH-TECH CORP.]
Modular Pre-Analytics2014-11-24
Hitachi High-Technologies Corp., Omuta Center [HITACHI HIGH-TECH CORP.]
e4112014-11-04
Hitachi High-Technologies Corp., Omuta Center [HITACHI HIGH-TECH CORP.]
MODULAR E2014-11-04
Hitachi High-Technologies Corp., Omuta Center [HITACHI HIGH-TECH CORP.]
ELECSYS 2010 ANALYZER2014-11-04

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