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FDA 510(k)

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)

K-Number: K250592 · 2025-05-12

Decision Date2025-05-12
Product CodeOWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) is a medical device manufactured by Northeast Scientific, Inc.. It received FDA 510(k) clearance on 2025-05-12 under approval number K250592. The device is classified under product code OWQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)?

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) is a medical device that received FDA 510(k) clearance on 2025-05-12. It is manufactured by Northeast Scientific, Inc.. The 510(k) number is K250592.

When was NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) approved by the FDA?

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) received FDA 510(k) clearance on 2025-05-12, under approval number K250592.

What company makes NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)?

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) is manufactured by Northeast Scientific, Inc..

What is the FDA product code for NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)?

The FDA product code for NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) is OWQ.

Other Devices by Northeast Scientific, Inc.

Related Devices (Code: OWQ)

Official Source

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