Medical Device Manufacturer · US , Pl. Grove , UT

R. Kent Richards, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1985

12

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - R. Kent Richards, Inc. Microbiology ✕

12 devices

1-12 of 12

Cleared Apr 14, 1987

CHLAMYDIA & VIRAL TRANSPORT MEDIUM

Microbiology · 27d

Cleared Nov 18, 1985

HEKTOEN ENTERIC AGAR

Microbiology · 13d

Cleared Nov 18, 1985

BILE ESCULIN AZIDE AGAR

Microbiology · 13d

Cleared Nov 18, 1985

MUELLER HINTON MEDIUM

Microbiology · 13d

Cleared Nov 18, 1985

MANNITOL SALT AGAR

Microbiology · 13d

Cleared Nov 18, 1985

P.E.Z. AGAR (PHENYLETHANOL AGAR)

Microbiology · 13d

Cleared Nov 18, 1985

TRYPTIC SOY BLOOD AGAR

Microbiology · 13d

Cleared Nov 18, 1985

CDC ANAEROBE BLOOD AGAR

Microbiology · 13d

Cleared Nov 18, 1985

CAMPYLOBACTER BLOOD AGAR

Microbiology · 13d

Cleared Nov 18, 1985

COLUMBIA CNA AGAR W/5% SHEEP BLOOD

Microbiology · 13d

Cleared Nov 12, 1985

THAYER-MARTIN MEDIUM (MOD)

Microbiology · 25d

Cleared Oct 31, 1985

COLUMBIA 5% BLOOD AGAR

Microbiology · 13d