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FDA PMA

Lymph node location system during sentinel biopsy procedure

Número do PMA: P160053 · 2026-05-18

RequerenteEndomagnetics Ltd.,
Data da decisão2026-05-18
Número PMAP160053
Código do produtoPUV
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoSU

Resumo do dispositivo

Lymph node location system during sentinel biopsy procedure is the device name listed in this FDA 510(k) record. The listed applicant is Endomagnetics Ltd.,. It received FDA 510(k) clearance on 2026-05-18. The device is classified under product code PUV. It was reviewed by the SU advisory panel.

Perguntas frequentes

What is the Lymph node location system during sentinel biopsy procedure?

Lymph node location system during sentinel biopsy procedure is a medical device that received FDA 510(k) clearance on 2026-05-18. The listed applicant is Endomagnetics Ltd.,.

When did Lymph node location system during sentinel biopsy procedure receive FDA 510(k) clearance?

The clearance date for Lymph node location system during sentinel biopsy procedure can be found in the official FDA records.

Who is the listed applicant for Lymph node location system during sentinel biopsy procedure?

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

What is the FDA product code for Lymph node location system during sentinel biopsy procedure?

The FDA product code for Lymph node location system during sentinel biopsy procedure is PUV.

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