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FDA 510(k)

KLIGER IRON AGAR

K-Number: K844520 · 1985-01-07

ApplicantbioMerieux, Inc.
Decision Date1985-01-07
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

KLIGER IRON 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 1985-01-07 under 510(k) number K844520. 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 KLIGER IRON AGAR?

KLIGER IRON AGAR is a medical device that received FDA 510(k) clearance on 1985-01-07. The listed applicant is bioMerieux, Inc.. The 510(k) number is K844520.

When did KLIGER IRON AGAR receive FDA 510(k) clearance?

KLIGER IRON AGAR received FDA 510(k) clearance on 1985-01-07, under 510(k) number K844520.

Who is the listed applicant for KLIGER IRON 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 KLIGER IRON AGAR?

The FDA product code for KLIGER IRON 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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