Medical Device Manufacturer · US , Mchenry , IL

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

19 submissions · 19 cleared · Since 1979

Recent clearances: #2010 CAMPHYLOBACTER AGAR, #50002 QUAD DIAGNOSTIC SYSTEM, #50003 QUAD DIAGNOSTIC SYSTEM

19

Total

19

Cleared

0

Denied

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

9 devices

1-9 of 9

Cleared Jun 18, 1981

MUELLER HINTON AGAR

Toxicology · 23d

Cleared Jun 18, 1981

MUELLER HINTON AGAR, POURED INTO A PLATE

Toxicology · 23d

Cleared Jun 18, 1981

MUELLER HINTON AGAR W/5% SHEEP BLOOD

Toxicology · 23d

Cleared Jun 18, 1981

TRYPTIC SOY AGAR W/5% SHEEP BLOOD & EMB

Toxicology · 23d

Cleared Jun 18, 1981

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

Toxicology · 23d

Cleared Jun 18, 1981

THAYER MARTIN AGAR

Toxicology · 23d

Cleared Jun 18, 1981

Toxicology · 23d

Cleared Jun 18, 1981

EMB AGAR, LEVINE

Toxicology · 23d

Cleared Jun 18, 1981

CHODOLATE AGAR, ENRICHED

Toxicology · 23d