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FDA 510(k)

MUELLER HINTON SENSITIVITY PLATE

K-Number: K851518 · 1985-04-29

Decision Date1985-04-29
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUELLER HINTON SENSITIVITY PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Culture Kits, Inc.. It received FDA 510(k) clearance on 1985-04-29 under 510(k) number K851518. 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 SENSITIVITY PLATE?

MUELLER HINTON SENSITIVITY PLATE is a medical device that received FDA 510(k) clearance on 1985-04-29. The listed applicant is Culture Kits, Inc.. The 510(k) number is K851518.

When did MUELLER HINTON SENSITIVITY PLATE receive FDA 510(k) clearance?

MUELLER HINTON SENSITIVITY PLATE received FDA 510(k) clearance on 1985-04-29, under 510(k) number K851518.

Who is the listed applicant for MUELLER HINTON SENSITIVITY PLATE?

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

What is the FDA product code for MUELLER HINTON SENSITIVITY PLATE?

The FDA product code for MUELLER HINTON SENSITIVITY 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 Culture Kits, 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 9 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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