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FDA 510(k)

COCCIDIOIDES IMMITIS, ANTISERUM

K-Number: K792688 · 1980-01-17

Decision Date1980-01-17
Product CodeGMH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COCCIDIOIDES IMMITIS, ANTISERUM is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Diagnostics, Inc.. It received FDA 510(k) clearance on 1980-01-17 under 510(k) number K792688. The device is classified under product code GMH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COCCIDIOIDES IMMITIS, ANTISERUM?

COCCIDIOIDES IMMITIS, ANTISERUM is a medical device that received FDA 510(k) clearance on 1980-01-17. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K792688.

When did COCCIDIOIDES IMMITIS, ANTISERUM receive FDA 510(k) clearance?

COCCIDIOIDES IMMITIS, ANTISERUM received FDA 510(k) clearance on 1980-01-17, under 510(k) number K792688.

Who is the listed applicant for COCCIDIOIDES IMMITIS, ANTISERUM?

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

What is the FDA product code for COCCIDIOIDES IMMITIS, ANTISERUM?

The FDA product code for COCCIDIOIDES IMMITIS, ANTISERUM is GMH.

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 Meridian Diagnostics, 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 92 devices →

Related Devices (Code: GMH)

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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