FDA 510(k)

Medline ReNewal Reprocessed Endopath Endoscopic Instruments

N.º K: K152313 · 2016-01-06

SolicitanteSurgical Instrument Services and Savings, Inc.

Fecha de decisión2016-01-06

Código de productoNUJ

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Medline ReNewal Reprocessed Endopath Endoscopic Instruments 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 2016-01-06 under 510(k) number K152313. 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 Endopath Endoscopic Instruments?

Medline ReNewal Reprocessed Endopath Endoscopic Instruments is a medical device that received FDA 510(k) clearance on 2016-01-06. The listed applicant is Surgical Instrument Services and Savings, Inc.. The 510(k) number is K152313.

When did Medline ReNewal Reprocessed Endopath Endoscopic Instruments receive FDA 510(k) clearance?

Medline ReNewal Reprocessed Endopath Endoscopic Instruments received FDA 510(k) clearance on 2016-01-06, under 510(k) number K152313.

Who is the listed applicant for Medline ReNewal Reprocessed Endopath Endoscopic Instruments?

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 Endopath Endoscopic Instruments?

The FDA product code for Medline ReNewal Reprocessed Endopath Endoscopic Instruments is NUJ.

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

K232130Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheter K162751Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider

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 K191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLC K182588Medline 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.