CHROMID CARBA agar (CARB)

FDA 510(k) K181092 · Biomerieux S.A.

Substantially Equivalent

510(k) numberK181092

Submission

Device name
CHROMID CARBA agar (CARB)
Applicant
Biomerieux S.A.
Marcy-L'Etoile, FR
Received
April 25, 2018
Decision date
July 6, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JSO – Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar
Device class
Class II (moderate risk)
Regulation
21 CFR 866.1700
Specialty
Microbiology

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K190553HardyCHROM CREJSO · Traditional Hardy Diagnostics04/29/2019SE
K171061MRSASelect IIJSO · Traditional Bio-Rad12/28/2017SE
K162620Remel Spectra ESBLJSO · Traditional Remel, Inc.05/01/2017SE
K160512HardyCHROM ESBLJSO · Traditional Hardy Diagnostics11/15/2016SE
K162076chromID MRSAJSO · Traditional bioMerieux, Inc.10/25/2016SE
K151688chromID MRSAJSO · Traditional bioMerieux, Inc.03/11/2016SE
K122187Vreselect Culture MediumJSO · Traditional Bio-Rad11/06/2012SE
K103684Vreselect Culture MediumJSO · Traditional Bio-Rad10/21/2011SE
K102922Hardychrom MrsaJSO · Traditional Hardy Diagnostics05/04/2011SE
K100589Mrsa Select - Skin and Soft Tissue Wound SpecimensJSO · Traditional Bio-Rad10/29/2010SE

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Questions and answers

When was CHROMID CARBA agar (CARB) cleared by the FDA?

CHROMID CARBA agar (CARB) (K181092) received a 510(k) decision of Substantially Equivalent on July 6, 2018, 72 days after the submission was received.

What is the product code of K181092?

The FDA product code is JSO – Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar, a Class II (moderate risk) device regulated under 21 CFR 866.1700.