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FDA 510(k)

MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE

K-Number: K851589 · 1985-04-30

Decision Date1985-04-30
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE is the device name listed in this FDA 510(k) record. The listed applicant is Preferred Micro-Media. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K851589. The device is classified under product code JTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 28 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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