MUELLER HINTIN AGAR W/5% SHEEP BLOOD
K-Number: K800979 · 1980-05-23
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTIN AGAR W/5% SHEEP BLOOD?
MUELLER HINTIN AGAR W/5% SHEEP BLOOD is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Quality Assurance Laboratory, Inc.. The 510(k) number is K800979.
When did MUELLER HINTIN AGAR W/5% SHEEP BLOOD receive FDA 510(k) clearance?
MUELLER HINTIN AGAR W/5% SHEEP BLOOD received FDA 510(k) clearance on 1980-05-23, under 510(k) number K800979.
Who is the listed applicant for MUELLER HINTIN AGAR W/5% SHEEP BLOOD?
The FDA 510(k) record lists Quality Assurance Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTIN AGAR W/5% SHEEP BLOOD?
The FDA product code for MUELLER HINTIN 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 Quality Assurance Laboratory, 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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