FDA 510(k)

LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)

K-Number: K884208 · 1988-10-25

Decision Date1988-10-25

Product CodeKZI

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION) is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1988-10-25 under 510(k) number K884208. 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 LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)?

LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION) is a medical device that received FDA 510(k) clearance on 1988-10-25. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K884208.

When did LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION) receive FDA 510(k) clearance?

LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION) received FDA 510(k) clearance on 1988-10-25, under 510(k) number K884208.

Who is the listed applicant for LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)?

The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)?

The FDA product code for LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION) is KZI.

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Other records listing Oxoid U.S.A., Inc. as applicant

K891593LISTERIA SELECTIVE ENRICHMENT MEDIUM K884026ESCHERICHIA COLI 0157 LATEX AGGLUTINATION TEST KIT K874303STAPHYLASE TEST K872956SORBITOL MACCONKEY AGAR NO. 3 CM 813 K872135MCBRIDE MEDIUM CM 819 K870945RABBIT PLASMA FIBRINOGEN SUPPLEMENT SR 122

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Related Devices (Code: KZI)

K881995DIAMOND'S MEDIUM MODIFIEDRemel Co.K880131LOWENSTEIN-JENSEN, GRUFTHardy Media K880134MIDDLEBROOK 7H11 AGARHardy Media K880122MIDDLEBROOK 7H9 BROTHHardy Media K880138WALLENSTEIN MEDIUM SLANTHardy Media K880109CYSTINE TRYPTIC MEDIUM BASEHardy 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.