Medical Device Manufacturer · US , Mchenry , IL

Immulok, Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1981

Total

Cleared

Denied

Immulok, Inc. has 15 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1981 to 1983. Primary specialty: Microbiology.

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

FDA 510(k) Regulatory Record - Immulok, Inc.

15 devices

1-12 of 15

Cleared Jun 30, 1983

HERPES SIMPLEX VIRUS TYPING REAGENTS

K830971 · GQL

Microbiology · 94d

Cleared May 04, 1983

CULUTURE SET CHLAMYDIA ISOLATION AND

RIASET PROLACTIN RIA KIT

K823304 · CFT

Chemistry · 47d

Cleared Nov 29, 1982

FLUOROSET IMMUNOFLUORESCENT ANTIBODY

K822785 · GQL

Microbiology · 76d

Cleared Nov 05, 1982

FLOUROSET IMMUNOFLUORESCENT ANTIBODY

K823055 · DHN

Immunology · 18d

Cleared Nov 01, 1982

CYTOMEGALOVIRUS ANTOBODY IGG

K822606 · LIN

Microbiology · 66d

Cleared Oct 27, 1982

TOXOPLASMA GONDII ANTIBODY IGG

K822605 · LJK

Microbiology · 61d

Cleared Sep 17, 1982

ANTINUCLEAR ANTOBODY CELL SUBSTRATE

K822607 · DHN

Immunology · 21d

Cleared Jun 25, 1982

HISTOSET IMMUNOPEROFIDASE TISSUE

HISTOSET IMMUNOPEROXIDASE TISSURE KIT

K820390 · LKH

Chemistry · 63d

Immulok, Inc. - FDA 510(k) Cleared Devices

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