BACTEROIDES BILE ESCULIN GAR
K-Number: K841222 · 1984-04-04
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Device Summary
Frequently Asked Questions
What is the BACTEROIDES BILE ESCULIN GAR?
BACTEROIDES BILE ESCULIN GAR is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Anaerobe Systems. The 510(k) number is K841222.
When did BACTEROIDES BILE ESCULIN GAR receive FDA 510(k) clearance?
BACTEROIDES BILE ESCULIN GAR received FDA 510(k) clearance on 1984-04-04, under 510(k) number K841222.
Who is the listed applicant for BACTEROIDES BILE ESCULIN GAR?
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 BACTEROIDES BILE ESCULIN GAR?
The FDA product code for BACTEROIDES BILE ESCULIN GAR 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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