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FDA 510(k)

BRILLIANT GREEN AGAR

K-Number: K871094 · 1987-04-03

ApplicantbioMerieux, Inc.
Decision Date1987-04-03
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BRILLIANT GREEN AGAR is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1987-04-03 under 510(k) number K871094. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRILLIANT GREEN AGAR?

BRILLIANT GREEN AGAR is a medical device that received FDA 510(k) clearance on 1987-04-03. The listed applicant is bioMerieux, Inc.. The 510(k) number is K871094.

When did BRILLIANT GREEN AGAR receive FDA 510(k) clearance?

BRILLIANT GREEN AGAR received FDA 510(k) clearance on 1987-04-03, under 510(k) number K871094.

Who is the listed applicant for BRILLIANT GREEN AGAR?

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

What is the FDA product code for BRILLIANT GREEN AGAR?

The FDA product code for BRILLIANT GREEN AGAR is JSI.

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Related Devices (Code: JSI)

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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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