Louise Miyamoto

FDA Filings

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

FDA Registration(s)
Registration Number3004569406
FEI Number3004569406
NameLouise Miyamoto
Owner & OperatorBiomerica, Inc.
Contact Address17571 Von Karman Ave --
Irvine CA 92614 US
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address17571 Von Karman Ave
Irvine, CA 92614 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Louise Miyamoto [Biomerica, Inc.]
Microalbumin2018-11-01
Louise Miyamoto [Biomerica, Inc.]
Fortel Microalbumin Screening2018-11-01
Louise Miyamoto [Biomerica, Inc.]
Giardia Lateral Flow Rapid Test2016-11-07
Louise Miyamoto [Biomerica, Inc.]
C. difficile (GDH)2016-11-07
Louise Miyamoto [Biomerica, Inc.]
Listeria Lateral Flow Rapid Test2016-11-07
Louise Miyamoto [Biomerica, Inc.]
Salmonella Lateral Flow Rapid Test2016-11-07
Louise Miyamoto [Biomerica, Inc.]
Shigella Lateral Flow Rapid Test2016-11-07
Louise Miyamoto [Biomerica, Inc.]
EZ HCG2009-03-05
Louise Miyamoto [Biomerica, Inc.]
Aware Breast Pad2009-03-02
Louise Miyamoto [Biomerica, Inc.]
MODIFIED EZ DETECT OCC2001-01-16
Louise Miyamoto [Biomerica, Inc.]
LH Lateral Flow Rapid Test1985-11-22
Louise Miyamoto [Biomerica, Inc.]
FORTEL OVULATION1985-11-22

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