CAMPYLOBACTER GROWTH SUPPLEMENT
K-Number: K800266 · 1980-03-12
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Device Summary
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.
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
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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