MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE
K-Number: K851589 · 1985-04-30
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE?
MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE is a medical device that received FDA 510(k) clearance on 1985-04-30. The listed applicant is Preferred Micro-Media. The 510(k) number is K851589.
When did MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE receive FDA 510(k) clearance?
MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE received FDA 510(k) clearance on 1985-04-30, under 510(k) number K851589.
Who is the listed applicant for MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE?
The FDA 510(k) record lists Preferred Micro-Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE?
The FDA product code for MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE 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 Preferred Micro-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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