This page includes the latest FDA filings for Lincoln Diagnostics Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 1450391 |
FEI Number | 1450391 |
Name | LINCOLN DIAGNOSTICS, INC. |
Owner & Operator | LINCOLN DIAGNOSTICS, INC. |
Contact Address | 240 E. HICKORY POINT RD. Decatur IL 62526 US |
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 240 E. HICKORY POINT RD. DECATUR, IL 62526 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
LINCOLN DIAGNOSTICS, INC. | Multi-Test PC | 2007-11-01 |
LINCOLN DIAGNOSTICS, INC. | Multi-Test II | 2007-11-01 |
LINCOLN DIAGNOSTICS, INC. | UniTest PC | 2007-11-01 |
LINCOLN DIAGNOSTICS, INC. | Duotip-Test | 2007-11-01 |
LINCOLN DIAGNOSTICS, INC. | Duotip-Test II | 2007-11-01 |
LINCOLN DIAGNOSTICS, INC. | Multi-Test | 2007-11-01 |
LINCOLN DIAGNOSTICS, INC. | MULTI-TEST II | 1996-08-07 |
LINCOLN DIAGNOSTICS, INC. | DUOTIP-TEST | 1994-09-02 |
NCAGE Code | 1Z310 | LINCOLN DIAGNOSTICS, INC. |
CAGE Code | 1Z310 | LINCOLN DIAGNOSTICS, INC. |
S.A.M. Registration | 1Z310 [54220009] | LINCOLN DIAGNOSTICS, INC. |