FDA 510(k)

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)

Número K: K220411 · 2022-05-13

RequerenteStryker Sustainability Solutions

Data da decisão2022-05-13

Código do produtoNUJ

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2022-05-13 under 510(k) number K220411. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is a medical device that received FDA 510(k) clearance on 2022-05-13. The listed applicant is Stryker Sustainability Solutions. The 510(k) number is K220411.

When did Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) receive FDA 510(k) clearance?

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) received FDA 510(k) clearance on 2022-05-13, under 510(k) number K220411.

Who is the listed applicant for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?

The FDA 510(k) record lists Stryker Sustainability Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?

The FDA product code for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is NUJ.

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Fonte oficial

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