XYLOSE LYSINE DESOXYCHOLATE AGAR
K-Number: K841131 · 1984-03-23
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Device Summary
Frequently Asked Questions
What is the XYLOSE LYSINE DESOXYCHOLATE AGAR?
XYLOSE LYSINE DESOXYCHOLATE AGAR is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Anaerobe Systems. The 510(k) number is K841131.
When did XYLOSE LYSINE DESOXYCHOLATE AGAR receive FDA 510(k) clearance?
XYLOSE LYSINE DESOXYCHOLATE AGAR received FDA 510(k) clearance on 1984-03-23, under 510(k) number K841131.
Who is the listed applicant for XYLOSE LYSINE DESOXYCHOLATE 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 XYLOSE LYSINE DESOXYCHOLATE AGAR?
The FDA product code for XYLOSE LYSINE DESOXYCHOLATE 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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