Lincoln Diagnostics Inc

FDA Filings

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.

FDA Registration(s)
Registration Number1450391
FEI Number1450391
NameLINCOLN DIAGNOSTICS, INC.
Owner & OperatorLINCOLN DIAGNOSTICS, INC.
Contact Address240 E. HICKORY POINT RD.
Decatur IL 62526 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address240 E. HICKORY POINT RD.
DECATUR, IL 62526 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
LINCOLN DIAGNOSTICS, INC.
Multi-Test PC2007-11-01
LINCOLN DIAGNOSTICS, INC.
Multi-Test II2007-11-01
LINCOLN DIAGNOSTICS, INC.
UniTest PC2007-11-01
LINCOLN DIAGNOSTICS, INC.
Duotip-Test2007-11-01
LINCOLN DIAGNOSTICS, INC.
Duotip-Test II2007-11-01
LINCOLN DIAGNOSTICS, INC.
Multi-Test2007-11-01
LINCOLN DIAGNOSTICS, INC.
MULTI-TEST II1996-08-07
LINCOLN DIAGNOSTICS, INC.
DUOTIP-TEST1994-09-02

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