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FDA 510(k)

COCCIDIOIDES ANTIGEN #CF10023X

K-Number: K791389 · 1979-08-16

Decision Date1979-08-16
Product CodeGMI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COCCIDIOIDES ANTIGEN #CF10023X is the device name listed in this FDA 510(k) record. The listed applicant is Immuno-Mycologics, Inc.. It received FDA 510(k) clearance on 1979-08-16 under 510(k) number K791389. The device is classified under product code GMI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COCCIDIOIDES ANTIGEN #CF10023X?

COCCIDIOIDES ANTIGEN #CF10023X is a medical device that received FDA 510(k) clearance on 1979-08-16. The listed applicant is Immuno-Mycologics, Inc.. The 510(k) number is K791389.

When did COCCIDIOIDES ANTIGEN #CF10023X receive FDA 510(k) clearance?

COCCIDIOIDES ANTIGEN #CF10023X received FDA 510(k) clearance on 1979-08-16, under 510(k) number K791389.

Who is the listed applicant for COCCIDIOIDES ANTIGEN #CF10023X?

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

What is the FDA product code for COCCIDIOIDES ANTIGEN #CF10023X?

The FDA product code for COCCIDIOIDES ANTIGEN #CF10023X is GMI.

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 Immuno-Mycologics, 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 26 devices →

Related Devices (Code: GMI)

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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