FDA 510(k)

Quidel Triage® TOX Drug Screen, 94600

Número K: K200363 · 2020-03-11

Data da decisão2020-03-11

Código do produtoDKZ

Comité consultivoTX

DecisãoSubstantially Equivalent

Resumo do dispositivo

Quidel Triage® TOX Drug Screen, 94600 is the device name listed in this FDA 510(k) record. The listed applicant is Quidel Cardiovascular, Inc.. It received FDA 510(k) clearance on 2020-03-11 under 510(k) number K200363. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Quidel Triage® TOX Drug Screen, 94600?

Quidel Triage® TOX Drug Screen, 94600 is a medical device that received FDA 510(k) clearance on 2020-03-11. The listed applicant is Quidel Cardiovascular, Inc.. The 510(k) number is K200363.

When did Quidel Triage® TOX Drug Screen, 94600 receive FDA 510(k) clearance?

Quidel Triage® TOX Drug Screen, 94600 received FDA 510(k) clearance on 2020-03-11, under 510(k) number K200363.

Who is the listed applicant for Quidel Triage® TOX Drug Screen, 94600?

The FDA 510(k) record lists Quidel Cardiovascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Quidel Triage® TOX Drug Screen, 94600?

The FDA product code for Quidel Triage® TOX Drug Screen, 94600 is DKZ.

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Outros registros que listam Quidel Cardiovascular, Inc. como candidato(a)

K182719Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterPro

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Fonte oficial

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