FDA 510(k)

ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL)

K-Number: K760834 · 1976-11-01

Decision Date1976-11-01

Product CodeGMH

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL) is the device name listed in this FDA 510(k) record. The listed applicant is I M, Inc.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760834. 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 ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL)?

ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL) is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is I M, Inc.. The 510(k) number is K760834.

When did ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL) receive FDA 510(k) clearance?

ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL) received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760834.

Who is the listed applicant for ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL)?

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

What is the FDA product code for ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL)?

The FDA product code for ANTI-COCCIDIOIDES CONT. SER. (MYCELIAL) is GMH.

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Related Devices (Code: GMH)

K792717COCCIDIOIDES IMMITIS, ANTISERUM POS.Meridian Diagnostics, Inc.K792688COCCIDIOIDES IMMITIS, ANTISERUMMeridian Diagnostics, Inc.K792684COCCIDIOIDES IMMITIS, ANTISERUM,Meridian Diagnostics, Inc.K791388ANTI-COCCIDIOIDES SERUM #CF10028XImmuno-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.