MUELLER HINTON AGAR, POURED INTO A PLATE
K-Number: K811472 · 1981-06-18
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR, POURED INTO A PLATE?
MUELLER HINTON AGAR, POURED INTO A PLATE is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Biomedia, Inc.. The 510(k) number is K811472.
When did MUELLER HINTON AGAR, POURED INTO A PLATE receive FDA 510(k) clearance?
MUELLER HINTON AGAR, POURED INTO A PLATE received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811472.
Who is the listed applicant for MUELLER HINTON AGAR, POURED INTO A PLATE?
The FDA 510(k) record lists Biomedia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR, POURED INTO A PLATE?
The FDA product code for MUELLER HINTON AGAR, POURED INTO A PLATE 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 Biomedia, 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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