Triever Catheters
K-Number: K210195 · 2021-02-24
Device Summary
Frequently Asked Questions
What is the Triever Catheters?
Triever Catheters is a medical device that received FDA 510(k) clearance on 2021-02-24. It is manufactured by Inari Medical. The 510(k) number is K210195.
When was Triever Catheters approved by the FDA?
Triever Catheters received FDA 510(k) clearance on 2021-02-24, under approval number K210195.
What company makes Triever Catheters?
Triever Catheters is manufactured by Inari Medical.
What is the FDA product code for Triever Catheters?
The FDA product code for Triever Catheters is QEW.
Related Clinical Trials
Other Devices by Inari Medical
Related Devices (Code: QEW)
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.