Medical Device Manufacturer · US , Mchenry , IL

Amico Lab, Inc. - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 1982

Total

Cleared

Denied

Amico Lab, Inc. has 32 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 32 cleared submissions from 1982 to 1985. Primary specialty: Microbiology.

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

Amico Lab, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Amico Lab, Inc.

32 devices

1-12 of 32

Cleared Dec 12, 1985

ANTI-EPSTEIN-BARR VIRUS KIT

AMIZYME-HSV TYPES 1 & 2 TEST KITS

K842531 · GQO

Immunology · 526d

Cleared Dec 06, 1985

ANTI-CYTOMEGALOVIRUS KIT

K842661 · GQI

Immunology · 514d

Cleared Dec 06, 1985

ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2

K842663 · GQO

Immunology · 514d

Cleared Oct 30, 1984

ANTI-SCHISTOSOMA SPECIES KIT

K842660 · GNH

Immunology · 112d

Cleared Oct 01, 1984

AMIZYME-C TRACHOMATIS TEST KIT

K842525 · LJP

Immunology · 95d

Cleared Oct 01, 1984

ANTI-CHLAMYDIA TRACHOMATIS KIT

AMIZYME-ANDNA TEST KIT

K842533 · LJM

Immunology · 84d

Cleared Sep 07, 1984

AMIZYME-TOXOPLASMA GONDII KIT

K842528 · LGD

Microbiology · 71d

Amico Lab, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Amico Lab, Inc.

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