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FDA 510(k)

CAMPYLOBACTER GROWTH SUPPLEMENT

K-Number: K800266 · 1980-03-12

Decision Date1980-03-12
Product CodeJSK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CAMPYLOBACTER GROWTH SUPPLEMENT 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 1980-03-12 under 510(k) number K800266. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPYLOBACTER GROWTH SUPPLEMENT?

CAMPYLOBACTER GROWTH SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K800266.

When did CAMPYLOBACTER GROWTH SUPPLEMENT receive FDA 510(k) clearance?

CAMPYLOBACTER GROWTH SUPPLEMENT received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800266.

Who is the listed applicant for CAMPYLOBACTER GROWTH SUPPLEMENT?

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 CAMPYLOBACTER GROWTH SUPPLEMENT?

The FDA product code for CAMPYLOBACTER GROWTH SUPPLEMENT is JSK.

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: JSK)

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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