Etest Voriconazole 0.002-32 Ug/Ml

FDA 510(k) K082534 · Ab Biomerieux

Substantially Equivalent

510(k) numberK082534

Submission

Device name
Etest Voriconazole 0.002-32 Ug/Ml
Applicant
Ab Biomerieux
Solna, SE
Received
September 2, 2008
Decision date
November 2, 2009
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
NGZ – Susceptibility Test Plate, Antifungal
Device class
Class II (moderate risk)
Regulation
21 CFR 866.1640
Specialty
Microbiology

The device is an in vitro diagnostic device intended for use in determining quantitative susceptibility of Candida species to various antifungal agents diluted in varying concentration in a microtiter plate format.

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Questions and answers

When was Etest Voriconazole 0.002-32 Ug/Ml cleared by the FDA?

Etest Voriconazole 0.002-32 Ug/Ml (K082534) received a 510(k) decision of Substantially Equivalent on November 2, 2009, 426 days after the submission was received.

What is the product code of K082534?

The FDA product code is NGZ – Susceptibility Test Plate, Antifungal, a Class II (moderate risk) device regulated under 21 CFR 866.1640.