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FDA 510(k)

Triever24, Triever20

K-Number: K213402 · 2022-05-23

ApplicantInari Medical
Decision Date2022-05-23
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Triever24, Triever20 is a medical device manufactured by Inari Medical. It received FDA 510(k) clearance on 2022-05-23 under approval number K213402. 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 Triever24, Triever20?

Triever24, Triever20 is a medical device that received FDA 510(k) clearance on 2022-05-23. It is manufactured by Inari Medical. The 510(k) number is K213402.

When was Triever24, Triever20 approved by the FDA?

Triever24, Triever20 received FDA 510(k) clearance on 2022-05-23, under approval number K213402.

What company makes Triever24, Triever20?

Triever24, Triever20 is manufactured by Inari Medical.

What is the FDA product code for Triever24, Triever20?

The FDA product code for Triever24, Triever20 is QEW.

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Related Devices (Code: QEW)

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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.

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