AV Vascular
K-Number: K253735 · 2026-01-22
Decision Date2026-01-22
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
AV Vascular is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2026-01-22 under approval number K253735. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AV Vascular?
AV Vascular is a medical device that received FDA 510(k) clearance on 2026-01-22. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K253735.
When was AV Vascular approved by the FDA?
AV Vascular received FDA 510(k) clearance on 2026-01-22, under approval number K253735.
What company makes AV Vascular?
AV Vascular is manufactured by Philips Medical Systems Nederland B.V..
What is the FDA product code for AV Vascular?
The FDA product code for AV Vascular is QIH.
Other Devices by Philips Medical Systems Nederland B.V.
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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.