ANAEROBIC BLOOD AGAR (CDC FORMULATION)
K-Number: K871089 · 1987-04-03
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Device Summary
Frequently Asked Questions
What is the ANAEROBIC BLOOD AGAR (CDC FORMULATION)?
ANAEROBIC BLOOD AGAR (CDC FORMULATION) is a medical device that received FDA 510(k) clearance on 1987-04-03. The listed applicant is bioMerieux, Inc.. The 510(k) number is K871089.
When did ANAEROBIC BLOOD AGAR (CDC FORMULATION) receive FDA 510(k) clearance?
ANAEROBIC BLOOD AGAR (CDC FORMULATION) received FDA 510(k) clearance on 1987-04-03, under 510(k) number K871089.
Who is the listed applicant for ANAEROBIC BLOOD AGAR (CDC FORMULATION)?
The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANAEROBIC BLOOD AGAR (CDC FORMULATION)?
The FDA product code for ANAEROBIC BLOOD AGAR (CDC FORMULATION) is JSG.
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 bioMerieux, 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: JSG)
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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