CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR
K-Number: K841218 · 1984-04-05
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Device Summary
Frequently Asked Questions
What is the CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR?
CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Anaerobe Systems. The 510(k) number is K841218.
When did CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR receive FDA 510(k) clearance?
CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR received FDA 510(k) clearance on 1984-04-05, under 510(k) number K841218.
Who is the listed applicant for CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR?
The FDA 510(k) record lists Anaerobe Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR?
The FDA product code for CYCLOSERINE-CEFOXITIN FRUCTOSE AGAR 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 Anaerobe Systems 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: 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
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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