ANAEROBIC BRUCELLA BLOOD AGAR
K-Number: K791579 · 1979-09-17
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Device Summary
Frequently Asked Questions
What is the ANAEROBIC BRUCELLA BLOOD AGAR?
ANAEROBIC BRUCELLA BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Anaerobe Systems. The 510(k) number is K791579.
When did ANAEROBIC BRUCELLA BLOOD AGAR receive FDA 510(k) clearance?
ANAEROBIC BRUCELLA BLOOD AGAR received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791579.
Who is the listed applicant for ANAEROBIC BRUCELLA BLOOD 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 ANAEROBIC BRUCELLA BLOOD AGAR?
The FDA product code for ANAEROBIC BRUCELLA BLOOD 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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