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.
Registration Number | 3004569406 |
FEI Number | 3004569406 |
Name | Louise Miyamoto |
Owner & Operator | Biomerica, Inc. |
Contact Address | 17571 Von Karman Ave -- Irvine CA 92614 US |
US Agent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 17571 Von Karman Ave Irvine, CA 92614 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
Louise Miyamoto [Biomerica, Inc.] | Microalbumin | 2018-11-01 |
Louise Miyamoto [Biomerica, Inc.] | Fortel Microalbumin Screening | 2018-11-01 |
Louise Miyamoto [Biomerica, Inc.] | Giardia Lateral Flow Rapid Test | 2016-11-07 |
Louise Miyamoto [Biomerica, Inc.] | C. difficile (GDH) | 2016-11-07 |
Louise Miyamoto [Biomerica, Inc.] | Listeria Lateral Flow Rapid Test | 2016-11-07 |
Louise Miyamoto [Biomerica, Inc.] | Salmonella Lateral Flow Rapid Test | 2016-11-07 |
Louise Miyamoto [Biomerica, Inc.] | Shigella Lateral Flow Rapid Test | 2016-11-07 |
Louise Miyamoto [Biomerica, Inc.] | EZ HCG | 2009-03-05 |
Louise Miyamoto [Biomerica, Inc.] | Aware Breast Pad | 2009-03-02 |
Louise Miyamoto [Biomerica, Inc.] | MODIFIED EZ DETECT OCC | 2001-01-16 |
Louise Miyamoto [Biomerica, Inc.] | LH Lateral Flow Rapid Test | 1985-11-22 |
Louise Miyamoto [Biomerica, Inc.] | FORTEL OVULATION | 1985-11-22 |