FDA 510(k)

HARMONIC 700 Shears

Número K: K221790 · 2023-02-28

Data da decisão2023-02-28

Código do produtoLFL

DecisãoSubstantially Equivalent

Resumo do dispositivo

HARMONIC 700 Shears is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2023-02-28 under 510(k) number K221790. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the HARMONIC 700 Shears?

HARMONIC 700 Shears is a medical device that received FDA 510(k) clearance on 2023-02-28. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K221790.

When did HARMONIC 700 Shears receive FDA 510(k) clearance?

HARMONIC 700 Shears received FDA 510(k) clearance on 2023-02-28, under 510(k) number K221790.

Who is the listed applicant for HARMONIC 700 Shears?

The FDA 510(k) record lists Ethicon Endo-Surgery, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HARMONIC 700 Shears?

The FDA product code for HARMONIC 700 Shears is LFL.

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Fonte oficial

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