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FDA 510(k)

Triever Catheters

K-Number: K210195 · 2021-02-24

ApplicantInari Medical
Decision Date2021-02-24
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Triever Catheters is a medical device manufactured by Inari Medical. It received FDA 510(k) clearance on 2021-02-24 under approval number K210195. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.