FDA 510(k)

HemoScreen Hematology Analyzer

Número K: K240636 · 2024-05-02

Data da decisão2024-05-02

Código do produtoGKZ

Comité consultivoHE

DecisãoSubstantially Equivalent

Resumo do dispositivo

HemoScreen Hematology Analyzer is the device name listed in this FDA 510(k) record. The listed applicant is Pixcell Medical Technologies. It received FDA 510(k) clearance on 2024-05-02 under 510(k) number K240636. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the HemoScreen Hematology Analyzer?

HemoScreen Hematology Analyzer is a medical device that received FDA 510(k) clearance on 2024-05-02. The listed applicant is Pixcell Medical Technologies. The 510(k) number is K240636.

When did HemoScreen Hematology Analyzer receive FDA 510(k) clearance?

HemoScreen Hematology Analyzer received FDA 510(k) clearance on 2024-05-02, under 510(k) number K240636.

Who is the listed applicant for HemoScreen Hematology Analyzer?

The FDA 510(k) record lists Pixcell Medical Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HemoScreen Hematology Analyzer?

The FDA product code for HemoScreen Hematology Analyzer is GKZ.

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