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FDA 510(k)

CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP

K-Number: K840969 · 1984-04-13

Decision Date1984-04-13
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP is the device name listed in this FDA 510(k) record. The listed applicant is Chatham Biological. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K840969. 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 CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP?

CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Chatham Biological. The 510(k) number is K840969.

When did CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP receive FDA 510(k) clearance?

CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840969.

Who is the listed applicant for CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP?

The FDA 510(k) record lists Chatham Biological as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP?

The FDA product code for CULTURE MEDIA FOR ANTIMICROBIAL SUSCEP 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 Chatham Biological 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

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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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