Keith A Barritt

FDA Filings

This page includes the latest FDA filings for Keith A Barritt. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3010281549
FEI Number3010281549
NameKEITH A BARRITT
Owner & OperatorJ. MORITA MFG. CORP.
Contact Address680 HIGASHIHAMA MINAMI-CHO, FUSHIMI-KU
KYOTO JP-NOTA 612-8533 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1000 Maine Ave., S.W., Suite 1000
Washington, DC 20024 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
KEITH A BARRITT [J. MORITA MFG. CORP.]
TORQTECH2012-01-31
KEITH A BARRITT [J. MORITA MFG. CORP.]
Twinpower Turbine PAR series2008-01-15

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