Triever20 Curve Catheter
K-Number: K203333 · 2020-12-10
ApplicantInari Medical, Inc.
Decision Date2020-12-10
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Triever20 Curve Catheter is a medical device manufactured by Inari Medical, Inc.. It received FDA 510(k) clearance on 2020-12-10 under approval number K203333. 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 Triever20 Curve Catheter?
Triever20 Curve Catheter is a medical device that received FDA 510(k) clearance on 2020-12-10. It is manufactured by Inari Medical, Inc.. The 510(k) number is K203333.
When was Triever20 Curve Catheter approved by the FDA?
Triever20 Curve Catheter received FDA 510(k) clearance on 2020-12-10, under approval number K203333.
What company makes Triever20 Curve Catheter?
Triever20 Curve Catheter is manufactured by Inari Medical, Inc..
What is the FDA product code for Triever20 Curve Catheter?
The FDA product code for Triever20 Curve Catheter is 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.