MUELLER HINTON BROTH
K-Number: K842854 · 1984-08-17
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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 1984-08-17. The listed applicant is Anarobe Systems. The 510(k) number is K842854.
When did MUELLER HINTON BROTH receive FDA 510(k) clearance?
MUELLER HINTON BROTH received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842854.
Who is the listed applicant for MUELLER HINTON BROTH?
The FDA 510(k) record lists Anarobe Systems 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 Anarobe Systems 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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