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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 the device name listed in this FDA 510(k) record. The listed applicant is Inari Medical. It received FDA 510(k) clearance on 2022-05-23 under 510(k) 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. The listed applicant is Inari Medical. The 510(k) number is K213402.

When did Triever24, Triever20 receive FDA 510(k) clearance?

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

Who is the listed applicant for Triever24, Triever20?

The FDA 510(k) record lists Inari Medical as the applicant. This does not by itself establish the device manufacturer.

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)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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