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FDA 510(k)

LISTERIA SELECTIVE ENRICHMENT MEDIUM

K-Number: K891593 · 1989-06-09

Decision Date1989-06-09
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LISTERIA SELECTIVE ENRICHMENT MEDIUM 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 1989-06-09 under 510(k) number K891593. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LISTERIA SELECTIVE ENRICHMENT MEDIUM?

LISTERIA SELECTIVE ENRICHMENT MEDIUM is a medical device that received FDA 510(k) clearance on 1989-06-09. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K891593.

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

LISTERIA SELECTIVE ENRICHMENT MEDIUM received FDA 510(k) clearance on 1989-06-09, under 510(k) number K891593.

Who is the listed applicant for LISTERIA SELECTIVE ENRICHMENT MEDIUM?

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 ENRICHMENT MEDIUM?

The FDA product code for LISTERIA SELECTIVE ENRICHMENT MEDIUM is JSI.

Related Clinical Trials

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.

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

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.

View all 93 devices →

Related Devices (Code: JSI)

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.

Official Source

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

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