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FDA 510(k)

TrapLiner catheter

K-Number: K180088 · 2018-04-04

ApplicantVascular Solutions, Inc.
Decision Date2018-04-04
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TrapLiner catheter is a medical device manufactured by Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2018-04-04 under approval number K180088. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TrapLiner catheter?

TrapLiner catheter is a medical device that received FDA 510(k) clearance on 2018-04-04. It is manufactured by Vascular Solutions, Inc.. The 510(k) number is K180088.

When was TrapLiner catheter approved by the FDA?

TrapLiner catheter received FDA 510(k) clearance on 2018-04-04, under approval number K180088.

What company makes TrapLiner catheter?

TrapLiner catheter is manufactured by Vascular Solutions, Inc..

What is the FDA product code for TrapLiner catheter?

The FDA product code for TrapLiner catheter is DQY.

Other Devices by Vascular Solutions, Inc.

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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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