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FDA 510(k)

Magic Torque DLVR Guidewire

K-Number: K182315 · 2018-09-26

ApplicantBoston Scientific Corporation
Decision Date2018-09-26
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Magic Torque DLVR Guidewire is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2018-09-26 under approval number K182315. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Magic Torque DLVR Guidewire?

Magic Torque DLVR Guidewire is a medical device that received FDA 510(k) clearance on 2018-09-26. It is manufactured by Boston Scientific Corporation. The 510(k) number is K182315.

When was Magic Torque DLVR Guidewire approved by the FDA?

Magic Torque DLVR Guidewire received FDA 510(k) clearance on 2018-09-26, under approval number K182315.

What company makes Magic Torque DLVR Guidewire?

Magic Torque DLVR Guidewire is manufactured by Boston Scientific Corporation.

What is the FDA product code for Magic Torque DLVR Guidewire?

The FDA product code for Magic Torque DLVR Guidewire is DQX.

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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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