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FDA 510(k)

IDENTIFICATION STICKS OXIDASE

K-Number: K844887 · 1985-02-25

ApplicantOxoid U.S.A., Inc.
Decision Date1985-02-25
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IDENTIFICATION STICKS OXIDASE 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 1985-02-25 under 510(k) number K844887. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDENTIFICATION STICKS OXIDASE?

IDENTIFICATION STICKS OXIDASE is a medical device that received FDA 510(k) clearance on 1985-02-25. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K844887.

When did IDENTIFICATION STICKS OXIDASE receive FDA 510(k) clearance?

IDENTIFICATION STICKS OXIDASE received FDA 510(k) clearance on 1985-02-25, under 510(k) number K844887.

Who is the listed applicant for IDENTIFICATION STICKS OXIDASE?

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 IDENTIFICATION STICKS OXIDASE?

The FDA product code for IDENTIFICATION STICKS OXIDASE is JTO.

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

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K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMK884026ESCHERICHIA COLI 0157 LATEX AGGLUTINATION TEST KITK884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)K874303STAPHYLASE TESTK872956SORBITOL MACCONKEY AGAR NO. 3 CM 813K872135MCBRIDE MEDIUM CM 819

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Related Devices (Code: JTO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, Inc.

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.

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