R. Kent Richards, Inc.
R. Kent Richards, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1987.
Top product codes for R. Kent Richards, Inc.
Recent clearances by R. Kent Richards, Inc.
- K871065 — CHLAMYDIA & VIRAL TRANSPORT MEDIUM
- K854449 — HEKTOEN ENTERIC AGAR
- K854450 — BILE ESCULIN AZIDE AGAR
- K854451 — MUELLER HINTON MEDIUM
- K854452 — MANNITOL SALT AGAR
- K854453 — P.E.Z. AGAR (PHENYLETHANOL AGAR)
- K854454 — TRYPTIC SOY BLOOD AGAR
- K854455 — CDC ANAEROBE BLOOD AGAR
- K854456 — CAMPYLOBACTER BLOOD AGAR
- K854457 — COLUMBIA CNA AGAR W/5% SHEEP BLOOD
- K854275 — THAYER-MARTIN MEDIUM (MOD)
- K854228 — COLUMBIA 5% BLOOD AGAR
Data sourced from openFDA. This site is unofficial and independent of the FDA.