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FDA 510(k)

CHROMID VRE AGAR, MODEL: REF 43 851

K-Number: K091025 · 2010-03-02

ApplicantbioMerieux, Inc.
Decision Date2010-03-02
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHROMID VRE AGAR, MODEL: REF 43 851 is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 2010-03-02 under 510(k) number K091025. The device is classified under product code JSO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHROMID VRE AGAR, MODEL: REF 43 851?

CHROMID VRE AGAR, MODEL: REF 43 851 is a medical device that received FDA 510(k) clearance on 2010-03-02. The listed applicant is bioMerieux, Inc.. The 510(k) number is K091025.

When did CHROMID VRE AGAR, MODEL: REF 43 851 receive FDA 510(k) clearance?

CHROMID VRE AGAR, MODEL: REF 43 851 received FDA 510(k) clearance on 2010-03-02, under 510(k) number K091025.

Who is the listed applicant for CHROMID VRE AGAR, MODEL: REF 43 851?

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 CHROMID VRE AGAR, MODEL: REF 43 851?

The FDA product code for CHROMID VRE AGAR, MODEL: REF 43 851 is JSO.

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Related Devices (Code: JSO)

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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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