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FDA 510(k)

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider

N.º K: K162751 · 2017-05-01

SolicitanteSurgical Instrument Services and Savings, Inc.
Fecha de decisión2017-05-01
Código de productoNUJ
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument Services and Savings, Inc.. It received FDA 510(k) clearance on 2017-05-01 under 510(k) number K162751. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is a medical device that received FDA 510(k) clearance on 2017-05-01. The listed applicant is Surgical Instrument Services and Savings, Inc.. The 510(k) number is K162751.

When did Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider receive FDA 510(k) clearance?

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider received FDA 510(k) clearance on 2017-05-01, under 510(k) number K162751.

Who is the listed applicant for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

The FDA 510(k) record lists Surgical Instrument Services 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 Curved, Small Jaw Open Sealer/Divider?

The FDA product code for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is NUJ.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Otros registros que enlistan a Surgical Instrument Services and Savings, Inc. como solicitante

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K232130Medline ReNewal Reprocessed ViewFlex Xtra ICE CatheterK152313Medline ReNewal Reprocessed Endopath Endoscopic Instruments

Dispositivos relacionados (Código: NUJ)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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 SolutionsK220411Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK211203Green OR Reprocessed Aquamantys Bipolar SealerGreen Or, LLCK191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLCK182588Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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