COLUMBIA SHEEP BLOOD AGAR 5%
K-Number: K830075 · 1983-02-09
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Device Summary
Frequently Asked Questions
What is the COLUMBIA SHEEP BLOOD AGAR 5%?
COLUMBIA SHEEP BLOOD AGAR 5% is a medical device that received FDA 510(k) clearance on 1983-02-09. The listed applicant is bioMerieux, Inc.. The 510(k) number is K830075.
When did COLUMBIA SHEEP BLOOD AGAR 5% receive FDA 510(k) clearance?
COLUMBIA SHEEP BLOOD AGAR 5% received FDA 510(k) clearance on 1983-02-09, under 510(k) number K830075.
Who is the listed applicant for COLUMBIA SHEEP BLOOD AGAR 5%?
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 COLUMBIA SHEEP BLOOD AGAR 5%?
The FDA product code for COLUMBIA SHEEP BLOOD AGAR 5% 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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