FDA 510(k)

COLUMBIA 5% BLOOD AGAR

K-Number: K854228 · 1985-10-31

Decision Date1985-10-31

Product CodeKZI

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

COLUMBIA 5% BLOOD AGAR is the device name listed in this FDA 510(k) record. The listed applicant is R. Kent Richards, Inc.. It received FDA 510(k) clearance on 1985-10-31 under 510(k) number K854228. The device is classified under product code KZI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLUMBIA 5% BLOOD AGAR?

COLUMBIA 5% BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1985-10-31. The listed applicant is R. Kent Richards, Inc.. The 510(k) number is K854228.

When did COLUMBIA 5% BLOOD AGAR receive FDA 510(k) clearance?

COLUMBIA 5% BLOOD AGAR received FDA 510(k) clearance on 1985-10-31, under 510(k) number K854228.

Who is the listed applicant for COLUMBIA 5% BLOOD AGAR?

The FDA 510(k) record lists R. Kent Richards, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLUMBIA 5% BLOOD AGAR?

The FDA product code for COLUMBIA 5% BLOOD AGAR is KZI.

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Other records listing R. Kent Richards, Inc. as applicant

K871065CHLAMYDIA & VIRAL TRANSPORT MEDIUM K854450BILE ESCULIN AZIDE AGAR K854449HEKTOEN ENTERIC AGAR K854454TRYPTIC SOY BLOOD AGAR K854457COLUMBIA CNA AGAR W/5% SHEEP BLOOD K854452MANNITOL SALT AGAR

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Related Devices (Code: KZI)

K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)Oxoid U.S.A., Inc.K881995DIAMOND'S MEDIUM MODIFIEDRemel Co.K880131LOWENSTEIN-JENSEN, GRUFTHardy Media K880122MIDDLEBROOK 7H9 BROTHHardy Media K880134MIDDLEBROOK 7H11 AGARHardy Media K880138WALLENSTEIN MEDIUM SLANTHardy Media

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.