MUELLER-HINTON BROTH
K-Number: K841560 · 1984-05-07
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Device Summary
Frequently Asked Questions
What is the MUELLER-HINTON BROTH?
MUELLER-HINTON BROTH is a medical device that received FDA 510(k) clearance on 1984-05-07. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K841560.
When did MUELLER-HINTON BROTH receive FDA 510(k) clearance?
MUELLER-HINTON BROTH received FDA 510(k) clearance on 1984-05-07, under 510(k) number K841560.
Who is the listed applicant for MUELLER-HINTON BROTH?
The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER-HINTON BROTH?
The FDA product code for MUELLER-HINTON BROTH 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 Gibco Laboratories Life Technologies, 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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