NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)
K-Number: K250592 · 2025-05-12
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.