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FDA 510(k)

MR Wire Guide Wire Straight, MR Wire Guide Wire Angled

K-Number: K173423 · 2017-11-17

ApplicantNano4imaging GmbH
Decision Date2017-11-17
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MR Wire Guide Wire Straight, MR Wire Guide Wire Angled is a medical device manufactured by Nano4imaging GmbH. It received FDA 510(k) clearance on 2017-11-17 under approval number K173423. 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 MR Wire Guide Wire Straight, MR Wire Guide Wire Angled?

MR Wire Guide Wire Straight, MR Wire Guide Wire Angled is a medical device that received FDA 510(k) clearance on 2017-11-17. It is manufactured by Nano4imaging GmbH. The 510(k) number is K173423.

When was MR Wire Guide Wire Straight, MR Wire Guide Wire Angled approved by the FDA?

MR Wire Guide Wire Straight, MR Wire Guide Wire Angled received FDA 510(k) clearance on 2017-11-17, under approval number K173423.

What company makes MR Wire Guide Wire Straight, MR Wire Guide Wire Angled?

MR Wire Guide Wire Straight, MR Wire Guide Wire Angled is manufactured by Nano4imaging GmbH.

What is the FDA product code for MR Wire Guide Wire Straight, MR Wire Guide Wire Angled?

The FDA product code for MR Wire Guide Wire Straight, MR Wire Guide Wire Angled is DQX.

Other Devices by Nano4imaging GmbH

K160594MRWire Guide Wire K253262EmeryGlide™ (EG18008901)

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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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