This page includes the latest FDA filings for David G Davis. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3003385757 |
FEI Number | 3003385757 |
Name | David G. Davis |
Owner & Operator | BECKMAN COULTER, INC. |
Contact Address | 250 S. Kraemer Blvd -- Brea CA 92821 US |
Official Correspondent |
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US Agent |
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Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 250 S. Kraemer Blvd. Brea, CA 92821 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
David G. Davis [BECKMAN COULTER, INC.] | Estrone-sulfate RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | DHEA-S-7 RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | Ultra-sensitive Estradiol RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | Free Testosterone RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | Active Free Testosterone RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | Aldosterone RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | Active Aldosterone RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | Estrone RIA | 2017-12-07 |
David G. Davis [BECKMAN COULTER, INC.] | DHEA RIA | 2017-12-07 |