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FDA 510(k)

Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)

Número K: K232511 · 2024-04-29

RequerenteSurgical Instrument Service and Savings, Inc.
Data da decisão2024-04-29
Código do produtoNUJ
Comité consultivoSU
DecisãoSubstantially Equivalent

Resumo do dispositivo

Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019) is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument Service and Savings, Inc.. It received FDA 510(k) clearance on 2024-04-29 under 510(k) number K232511. 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 Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)?

Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019) is a medical device that received FDA 510(k) clearance on 2024-04-29. The listed applicant is Surgical Instrument Service and Savings, Inc.. The 510(k) number is K232511.

When did Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019) receive FDA 510(k) clearance?

Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019) received FDA 510(k) clearance on 2024-04-29, under 510(k) number K232511.

Who is the listed applicant for Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)?

The FDA 510(k) record lists Surgical Instrument Service and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)?

The FDA product code for Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019) is NUJ.

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Dispositivos Relacionados (Código: NUJ)

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Fonte oficial

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