Medical Device Manufacturer · US , Mchenry , IL

Micro-Bio-Logics - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1984

Total

Cleared

Denied

Micro-Bio-Logics has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1984 to 1987. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Micro-Bio-Logics Filter by specialty or product code using the sidebar.

Micro-Bio-Logics 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 - Micro-Bio-Logics

9 devices

1-9 of 9

Cleared Jun 17, 1987

LYFO KWIK(TM) RUS KIT

K870731 · JXA

Microbiology · 112d

Cleared Apr 18, 1986

LYFO-KWIK (TM) COAGULASE PLASMA

K861312 · JTL

Hematology · 10d

Cleared Apr 04, 1986

KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS

INDI KWIK (TM) CO/TWO KIT

K855198 · JTR

Microbiology · 18d

Cleared Jul 23, 1985

NEISSERIA - KWIK PLUS

ONO/CO-TWO (TM) SYSTEMS

K844014 · JTY

Microbiology · 19d

Cleared Jul 03, 1984

LYFO-DISK MICROORGANISMS

K842129 · JTR

Microbiology · 35d

Micro-Bio-Logics - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Micro-Bio-Logics

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