CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ
K-Number: K850832 · 1985-03-29
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Device Summary
Frequently Asked Questions
What is the CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ?
CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ is a medical device that received FDA 510(k) clearance on 1985-03-29. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K850832.
When did CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ receive FDA 510(k) clearance?
CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ received FDA 510(k) clearance on 1985-03-29, under 510(k) number K850832.
Who is the listed applicant for CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ?
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 BLOOD-FREE SELECTIVE AGAR BASEQ?
The FDA product code for CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ is JSJ.
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: JSJ)
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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