Vreselect Culture Medium

FDA 510(k) K122187 · Bio-Rad

Substantially Equivalent

510(k) numberK122187

Submission

Device name
Vreselect Culture Medium
Applicant
Bio-Rad
Beverly, MA, US
Received
July 24, 2012
Decision date
November 6, 2012
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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K162620Remel Spectra ESBLJSO · Traditional Remel, Inc.05/01/2017SE
K160512HardyCHROM ESBLJSO · Traditional Hardy Diagnostics11/15/2016SE
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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 Vreselect Culture Medium cleared by the FDA?

Vreselect Culture Medium (K122187) received a 510(k) decision of Substantially Equivalent on November 6, 2012, 105 days after the submission was received.

What is the product code of K122187?

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.