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FDA 510(k)

BBLCHROMAGAR MRSA

K-Number: K042812 · 2004-11-22

ApplicantBecton, Dickinson & CO
Decision Date2004-11-22
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BBLCHROMAGAR MRSA is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson & CO. It received FDA 510(k) clearance on 2004-11-22 under 510(k) number K042812. 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 BBLCHROMAGAR MRSA?

BBLCHROMAGAR MRSA is a medical device that received FDA 510(k) clearance on 2004-11-22. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K042812.

When did BBLCHROMAGAR MRSA receive FDA 510(k) clearance?

BBLCHROMAGAR MRSA received FDA 510(k) clearance on 2004-11-22, under 510(k) number K042812.

Who is the listed applicant for BBLCHROMAGAR MRSA?

The FDA 510(k) record lists Becton, Dickinson & CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BBLCHROMAGAR MRSA?

The FDA product code for BBLCHROMAGAR MRSA is JSO.

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Related Devices (Code: JSO)

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K190553HardyCHROM CREHardy DiagnosticsK181092CHROMID CARBA agar (CARB)Biomerieux S.A.K171061MRSASelect IIBio-RadK162620Remel Spectra ESBLRemel, Inc.K160512HardyCHROM ESBLHardy DiagnosticsK162076chromID MRSAbioMerieux, Inc.

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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