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FDA 510(k)

MUELLER HINTON AGAR SMALL

K-Number: K864245 · 1987-03-31

Decision Date1987-03-31
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUELLER HINTON AGAR SMALL is the device name listed in this FDA 510(k) record. The listed applicant is Mds Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K864245. 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 SMALL?

MUELLER HINTON AGAR SMALL is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864245.

When did MUELLER HINTON AGAR SMALL receive FDA 510(k) clearance?

MUELLER HINTON AGAR SMALL received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864245.

Who is the listed applicant for MUELLER HINTON AGAR SMALL?

The FDA 510(k) record lists Mds Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUELLER HINTON AGAR SMALL?

The FDA product code for MUELLER HINTON AGAR SMALL 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 Mds Laboratories, 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.

View all 21 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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