FDA 510(k)

SonoStik Guide Wire Introducer

Numéro K : K243061 · 2024-11-04

Date de décision2024-11-04

Code produitDYB

Comité consultatifCV

DécisionSubstantially Equivalent

Résumé du dispositif

SonoStik Guide Wire Introducer is the device name listed in this FDA 510(k) record. The listed applicant is Sonostik, LLC. It received FDA 510(k) clearance on 2024-11-04 under 510(k) number K243061. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the SonoStik Guide Wire Introducer?

SonoStik Guide Wire Introducer is a medical device that received FDA 510(k) clearance on 2024-11-04. The listed applicant is Sonostik, LLC. The 510(k) number is K243061.

When did SonoStik Guide Wire Introducer receive FDA 510(k) clearance?

SonoStik Guide Wire Introducer received FDA 510(k) clearance on 2024-11-04, under 510(k) number K243061.

Who is the listed applicant for SonoStik Guide Wire Introducer?

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

What is the FDA product code for SonoStik Guide Wire Introducer?

The FDA product code for SonoStik Guide Wire Introducer is DYB.

Essais cliniques associés

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Dispositifs connexes (Code : DYB)

K253526NAMIC Dilator and SheathMedline Industries, LP K261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLC K261242SimplGuidePendracare K261950Health Line Tearaway IntroducerHealth Line International Corporation K261492FieldFlex Steerable SheathCenterPoint Systems, LLC K260606Echo Large Bore Introducer SheathEcho Medical, LLC

Source officielle

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