MUELLER HINTON MEDIUM
K-Number: K821430 · 1982-06-01
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON MEDIUM?
MUELLER HINTON MEDIUM is a medical device that received FDA 510(k) clearance on 1982-06-01. The listed applicant is Interstate Media. The 510(k) number is K821430.
When did MUELLER HINTON MEDIUM receive FDA 510(k) clearance?
MUELLER HINTON MEDIUM received FDA 510(k) clearance on 1982-06-01, under 510(k) number K821430.
Who is the listed applicant for MUELLER HINTON MEDIUM?
The FDA 510(k) record lists Interstate Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON MEDIUM?
The FDA product code for MUELLER HINTON MEDIUM 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 Interstate Media 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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