Medical Device Manufacturer · US , Mchenry , IL

Lkb Instruments, Inc. - FDA 510(k) Cleared Devices

52 submissions · 52 cleared · Since 1976

Total

Cleared

Denied

Lkb Instruments, Inc. has 52 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 52 cleared submissions from 1976 to 1987. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Lkb Instruments, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lkb Instruments, Inc.

52 devices

1-12 of 52

Cleared Nov 04, 1987

1205 BETAPLATE LIQUID SCINTILLATION COUNTER

K874094 · JJJ

Chemistry · 35d

Cleared Aug 21, 1987

DELFIA(TM) FERRITIN KIT

K872955 · JMG

Microbiology · 23d

Cleared Jun 17, 1987

DELFIA(TM) THYROXINE (T4) KIT

DELFIA(TM) TRIIODOTHYRONINE (T3) KIT

LKB ULTROBACT (TM) PNEUMOCOCCUS KIT

K862848 · GWC

Microbiology · 142d

Cleared Sep 26, 1986

DELFIA(TM) CORTISOL KIT

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Lkb Instruments, Inc. - FDA 510(k) Cleared Devices

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