Medical Device Manufacturer · US , Mchenry , IL

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

19 submissions · 19 cleared · Since 1979

Total

Cleared

Denied

Biomedia, Inc. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 19 cleared submissions from 1979 to 1982. Primary specialty: Toxicology.

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

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

19 devices

1-19 of 19

Cleared Jun 02, 1982

#2010 CAMPHYLOBACTER AGAR

K821300 · JSI

Microbiology · 29d

Cleared Jun 01, 1982

#50002 QUAD DIAGNOSTIC SYSTEM

K821301 · JSI

Microbiology · 28d

Cleared Jun 01, 1982

#50003 QUAD DIAGNOSTIC SYSTEM

K821302 · JSH

Microbiology · 28d

Cleared May 13, 1982

BI PLATE-XLD/HEKTOEN #30012

MUELLER HINTON AGAR, POURED INTO A PLATE

K811472 · JTZ

Toxicology · 23d

Cleared Jun 18, 1981

MUELLER HINTON AGAR W/5% SHEEP BLOOD

K811473 · JTZ

Toxicology · 23d

Cleared Jun 18, 1981

TRYPTIC SOY AGAR W/5% SHEEP BLOOD & EMB

K811474 · JSI

Toxicology · 23d

Cleared Jun 18, 1981

TRYPTIC SOY AGAR W/5% & 10% SHEEP BLOOD

CHODOLATE AGAR, ENRICHED

K811479 · JTY

Toxicology · 23d

Cleared Sep 16, 1980

BACITRACIN DIFFERENTIATION DISC

K802127 · JTO

Microbiology · 13d

Cleared Oct 17, 1979

CULTURE AND SENSITIVITY KIT

K791413 · JTZ

Microbiology · 79d

Cleared Oct 17, 1979

DTM (DERMATOPHYTE TEST MEDIUM) AGAR

K791414 · JSI

Microbiology · 79d

Cleared Apr 23, 1979

EMB/MUELLER-HINTON AGAR

K790369 · JTZ

Pathology · 60d

Cleared Apr 04, 1979

STREP BLOOD AGAR-5% SHEEP BLOOD

K790469 · JSI

Chemistry · 30d

Cleared Mar 21, 1979

MODIFIED THAYER MARTIN AGAR

K790368 · JTY

Pathology · 27d

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

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