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FDA PMA

Processor, cervical cytology slide, automated

Número do PMA: P950039 · 2025-08-27

RequerenteHologic, Inc.
Data da decisão2025-08-27
Número PMAP950039
Código do produtoMKQ
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoPA

Resumo do dispositivo

Processor, cervical cytology slide, automated is the device name listed in this FDA 510(k) record. The listed applicant is Hologic, Inc.. It received FDA 510(k) clearance on 2025-08-27. The device is classified under product code MKQ. It was reviewed by the PA advisory panel.

Perguntas frequentes

What is the Processor, cervical cytology slide, automated?

Processor, cervical cytology slide, automated is a medical device that received FDA 510(k) clearance on 2025-08-27. The listed applicant is Hologic, Inc..

When did Processor, cervical cytology slide, automated receive FDA 510(k) clearance?

The clearance date for Processor, cervical cytology slide, automated can be found in the official FDA records.

Who is the listed applicant for Processor, cervical cytology slide, automated?

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

What is the FDA product code for Processor, cervical cytology slide, automated?

The FDA product code for Processor, cervical cytology slide, automated is MKQ.

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