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FDA 510(k)

ANTI-BLASTOMYCES SERUM #CF10027X

K-Number: K791390 · 1979-08-16

ApplicantImmuno-Mycologics, Inc.
Decision Date1979-08-16
Product CodeGMK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTI-BLASTOMYCES SERUM #CF10027X 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 K791390. The device is classified under product code GMK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-BLASTOMYCES SERUM #CF10027X?

ANTI-BLASTOMYCES SERUM #CF10027X 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 K791390.

When did ANTI-BLASTOMYCES SERUM #CF10027X receive FDA 510(k) clearance?

ANTI-BLASTOMYCES SERUM #CF10027X received FDA 510(k) clearance on 1979-08-16, under 510(k) number K791390.

Who is the listed applicant for ANTI-BLASTOMYCES SERUM #CF10027X?

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 ANTI-BLASTOMYCES SERUM #CF10027X?

The FDA product code for ANTI-BLASTOMYCES SERUM #CF10027X is GMK.

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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.

K120946ALPHA CRYPTOCOCCAL ANTIGEN EIAK112422CRAG LATERAL FLOW ASSAY (LFA)K102286CRAG LATERAL FLOW ASSAY (CRAG LFA)K101407ALPHA HISTOPLASMA ANTIGEN EIA MODEL HAG102K883333RABBIT PLASMA FIBRINOGEN (RPF) SUPPLEMENTK880029EXO-ANTIGEN IDENTIFICATION SYSTEM CAT.# EX1001

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Related Devices (Code: GMK)

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.

K792692IMMUNODIFFUSION BAND INTENSIFYING FLUIDMeridian Diagnostics, Inc.K792694NEGATIVE CONTROL SERUMMeridian Diagnostics, Inc.K792679HISTOPLASMA CAPSULATUM, ANTISERUMMeridian Diagnostics, Inc.K792718HISTOPLASMA CAPSULATUM, ANTISERUMMeridian Diagnostics, Inc.K791392ANTI-HISTOPLASMA SERUM #CF10026XImmuno-Mycologics, Inc.K791395ANTI-HISTOPLASMA SERUM #CF10025XImmuno-Mycologics, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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