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 |