MUELLER HINTON AGAR W/5% SHEEP BLOOD
K-Number: K811473 · 1981-06-18
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR W/5% SHEEP BLOOD?
MUELLER HINTON AGAR W/5% SHEEP BLOOD is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Biomedia, Inc.. The 510(k) number is K811473.
When did MUELLER HINTON AGAR W/5% SHEEP BLOOD receive FDA 510(k) clearance?
MUELLER HINTON AGAR W/5% SHEEP BLOOD received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811473.
Who is the listed applicant for MUELLER HINTON AGAR W/5% SHEEP BLOOD?
The FDA 510(k) record lists Biomedia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR W/5% SHEEP BLOOD?
The FDA product code for MUELLER HINTON AGAR W/5% SHEEP BLOOD is JTZ.
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 Biomedia, 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: JTZ)
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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