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

1-12 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

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

Filters