FDA 510(k)

Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter

Número K: K191073 · 2019-10-22

Data da decisão2019-10-22

Código do produtoNUJ

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Vein 360, LLC. It received FDA 510(k) clearance on 2019-10-22 under 510(k) number K191073. 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 Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter?

Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter is a medical device that received FDA 510(k) clearance on 2019-10-22. The listed applicant is Vein 360, LLC. The 510(k) number is K191073.

When did Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter receive FDA 510(k) clearance?

Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter received FDA 510(k) clearance on 2019-10-22, under 510(k) number K191073.

Who is the listed applicant for Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter?

The FDA 510(k) record lists Vein 360, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter?

The FDA product code for Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter is NUJ.

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Outros registros que listam Vein 360, LLC como candidato(a)

K232584Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter K230928Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter K230584Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter

Dispositivos Relacionados (Código: NUJ)

K232511Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)Surgical Instrument Service and Savings, Inc.K230251Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability Solutions K220411Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability Solutions K211203Green OR Reprocessed Aquamantys Bipolar SealerGreen Or, LLC K182588Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren K180499Reprocessed LigaSure Maryland Jaw Sealer/DividerStryker Sustainability Solutions

Fonte oficial

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