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FDA 510(k)

DTM AGAR

K-Number: K844514 · 1985-01-07

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

Device Summary

DTM 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 K844514. 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 DTM AGAR?

DTM 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 K844514.

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

DTM AGAR received FDA 510(k) clearance on 1985-01-07, under 510(k) number K844514.

Who is the listed applicant for DTM 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 DTM AGAR?

The FDA product code for DTM 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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