Class Class II

iNod Ultrasound Guided Biopsy Needle (UPN: M00502060), iNod Ultrasound Guidance Console (UPN: M00503210) (K221340)

K221340 2023-03-02 Traditional
Home/ Devices/ iNod Ultrasound Guided Biopsy…

Description

iNod Ultrasound Guided Biopsy Needle (UPN: M00502060), iNod Ultrasound Guidance Console (UPN: M00503210) by Boston Scientific Corporation, an FDA 510(k) cleared ear, nose, throat device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221340
Clearance Date2023-03-02
Clearance TypeTraditional
Product CodeEOQ
Regulation Number874.4680

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote

Predicate lineage for K221340

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. iNod Ultrasound Guided Biopsy Needle (UPN: M00502060), iNod Ultrasound Guidance Console (UPN: M00503210) (K221340) cites 4 predicate devices and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K212490AVVIGO Guidance System IIBoston Scientific Corporation2021
K203128EVIS EUS ENDOSCOPIC ULTRASOUND CENTER OLYMPUS EU-ME2/EVIS E...Olympus Medical Systems Corp.2020
K163537Arcpoint pulmonary needle - 18 ga, Arcpoint pulmonary needl...Covidien, LLC2017
K121564ENDOSCOPIC ULTRASOUND CENTER EU-Y0006Olympus Medical Systems Corp.2012

Trace the full predicate network for K221340

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

Scroll to Top