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FDA 510(k)

PRESTON CAMPYLOBACTER SELECTIVE SUPP

K-Number: K840330 · 1984-05-11

Decision Date1984-05-11
Product CodeJSK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PRESTON CAMPYLOBACTER SELECTIVE SUPP 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 1984-05-11 under 510(k) number K840330. 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 PRESTON CAMPYLOBACTER SELECTIVE SUPP?

PRESTON CAMPYLOBACTER SELECTIVE SUPP is a medical device that received FDA 510(k) clearance on 1984-05-11. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K840330.

When did PRESTON CAMPYLOBACTER SELECTIVE SUPP receive FDA 510(k) clearance?

PRESTON CAMPYLOBACTER SELECTIVE SUPP received FDA 510(k) clearance on 1984-05-11, under 510(k) number K840330.

Who is the listed applicant for PRESTON CAMPYLOBACTER SELECTIVE SUPP?

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 PRESTON CAMPYLOBACTER SELECTIVE SUPP?

The FDA product code for PRESTON CAMPYLOBACTER SELECTIVE SUPP 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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