MUELLER-HINTON
K-Number: K811608 · 1981-06-25
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Device Summary
Frequently Asked Questions
What is the MUELLER-HINTON?
MUELLER-HINTON is a medical device that received FDA 510(k) clearance on 1981-06-25. The listed applicant is Micro Media Laboratories. The 510(k) number is K811608.
When did MUELLER-HINTON receive FDA 510(k) clearance?
MUELLER-HINTON received FDA 510(k) clearance on 1981-06-25, under 510(k) number K811608.
Who is the listed applicant for MUELLER-HINTON?
The FDA 510(k) record lists Micro Media Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER-HINTON?
The FDA product code for MUELLER-HINTON 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 Micro Media Laboratories 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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