FDA 510(k)

Quest Diagnostics HairCheck-DT (Cocaine)

N.º K: K152232 · 2016-11-18

SolicitanteQuest Diagnostics Incorporated

Fecha de decisión2016-11-18

Código de productoDIO

Comité asesorTX

DecisiónSubstantially Equivalent

Resumen del dispositivo

Quest Diagnostics HairCheck-DT (Cocaine) is the device name listed in this FDA 510(k) record. The listed applicant is Quest Diagnostics Incorporated. It received FDA 510(k) clearance on 2016-11-18 under 510(k) number K152232. The device is classified under product code DIO. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Quest Diagnostics HairCheck-DT (Cocaine)?

Quest Diagnostics HairCheck-DT (Cocaine) is a medical device that received FDA 510(k) clearance on 2016-11-18. The listed applicant is Quest Diagnostics Incorporated. The 510(k) number is K152232.

When did Quest Diagnostics HairCheck-DT (Cocaine) receive FDA 510(k) clearance?

Quest Diagnostics HairCheck-DT (Cocaine) received FDA 510(k) clearance on 2016-11-18, under 510(k) number K152232.

Who is the listed applicant for Quest Diagnostics HairCheck-DT (Cocaine)?

The FDA 510(k) record lists Quest Diagnostics Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Quest Diagnostics HairCheck-DT (Cocaine)?

The FDA product code for Quest Diagnostics HairCheck-DT (Cocaine) is DIO.

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