Biomedia, Inc.
Biomedia, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1982.
Top product codes for Biomedia, Inc.
Recent clearances by Biomedia, Inc.
- K821300 — #2010 CAMPHYLOBACTER AGAR
- K821301 — #50002 QUAD DIAGNOSTIC SYSTEM
- K821302 — #50003 QUAD DIAGNOSTIC SYSTEM
- K821108 — BI PLATE-XLD/HEKTOEN #30012
- K811471 — MUELLER HINTON AGAR
- K811472 — MUELLER HINTON AGAR, POURED INTO A PLATE
- K811473 — MUELLER HINTON AGAR W/5% SHEEP BLOOD
- K811474 — TRYPTIC SOY AGAR W/5% SHEEP BLOOD & EMB
- K811475 — TRYPTIC SOY AGAR W/5% & 10% SHEEP BLOOD
- K811476 — THAYER MARTIN AGAR
- K811477 — MACCONKEY AGAR
- K811478 — EMB AGAR, LEVINE
- K811479 — CHODOLATE AGAR, ENRICHED
- K802127 — BACITRACIN DIFFERENTIATION DISC
- K791413 — CULTURE AND SENSITIVITY KIT
- K791414 — DTM (DERMATOPHYTE TEST MEDIUM) AGAR
- K790369 — EMB/MUELLER-HINTON AGAR
- K790469 — STREP BLOOD AGAR-5% SHEEP BLOOD
- K790368 — MODIFIED THAYER MARTIN AGAR
Data sourced from openFDA. This site is unofficial and independent of the FDA.