FDA 510(k)

ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2

Número K: K220801 · 2022-06-24

RequerenteAbbott Diagnostics Scarborough, Inc.

Data da decisão2022-06-24

Código do produtoOZE

Comité consultivoMI

DecisãoSubstantially Equivalent

Resumo do dispositivo

ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Diagnostics Scarborough, Inc.. It received FDA 510(k) clearance on 2022-06-24 under 510(k) number K220801. The device is classified under product code OZE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2?

ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2 is a medical device that received FDA 510(k) clearance on 2022-06-24. The listed applicant is Abbott Diagnostics Scarborough, Inc.. The 510(k) number is K220801.

When did ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2 receive FDA 510(k) clearance?

ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2 received FDA 510(k) clearance on 2022-06-24, under 510(k) number K220801.

Who is the listed applicant for ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2?

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

What is the FDA product code for ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2?

The FDA product code for ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2 is OZE.

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Outros registros que listam Abbott Diagnostics Scarborough, Inc. como candidato(a)

K262747ID NOW Influenza A & B 2; ID NOW RSV; ID NOW Strep A 2; ID NOW COVID-19 2.0 K250273BinaxNOW COVID-19 Ag Card K243518BinaxNOW™ COVID-19 Antigen Self Test K232775ID NOW Influenza A & B 2 K221925ID NOW COVID-19 2.0 K191534ID NOW Influenza A & B 2

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Dispositivos Relacionados (Código: OZE)

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