Medical Device Manufacturer · US , Pl. Grove , UT

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

12 submissions · 12 cleared · Since 1985

Total

Cleared

Denied

R. Kent Richards, Inc. has 12 FDA 510(k) cleared microbiology devices. Based in Pl. Grove, US.

Historical record: 12 cleared submissions from 1985 to 1987.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

R. Kent Richards, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

12 devices

1-12 of 12

Cleared Apr 14, 1987

CHLAMYDIA & VIRAL TRANSPORT MEDIUM

BILE ESCULIN AZIDE AGAR

K854450 · JSI

Microbiology · 13d

Cleared Nov 18, 1985

MUELLER HINTON MEDIUM

P.E.Z. AGAR (PHENYLETHANOL AGAR)

K854453 · JSJ

Microbiology · 13d

Cleared Nov 18, 1985

TRYPTIC SOY BLOOD AGAR

K854454 · KZI

Microbiology · 13d

Cleared Nov 18, 1985

CDC ANAEROBE BLOOD AGAR

K854455 · JSG

Microbiology · 13d

Cleared Nov 18, 1985

CAMPYLOBACTER BLOOD AGAR

K854456 · JSJ

Microbiology · 13d

Cleared Nov 18, 1985

COLUMBIA CNA AGAR W/5% SHEEP BLOOD

K854457 · JSJ

Microbiology · 13d

Cleared Nov 12, 1985

THAYER-MARTIN MEDIUM (MOD)

K854275 · JTY

Microbiology · 25d

Cleared Oct 31, 1985

COLUMBIA 5% BLOOD AGAR

K854228 · KZI

Microbiology · 13d

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

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

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