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FDA 510(k)

CLED AGAR

K-Number: K871095 · 1987-04-03

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

Device Summary

CLED 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 K871095. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLED AGAR?

CLED 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 K871095.

When did CLED AGAR receive FDA 510(k) clearance?

CLED AGAR received FDA 510(k) clearance on 1987-04-03, under 510(k) number K871095.

Who is the listed applicant for CLED 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 CLED AGAR?

The FDA product code for CLED AGAR is JSH.

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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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