FDA 510(k)

Hi-Torque Command 18 Guide Wire

K-Number: K172073 · 2017-08-25

Decision Date2017-08-25

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Hi-Torque Command 18 Guide Wire is a medical device manufactured by Abbott Vascular. It received FDA 510(k) clearance on 2017-08-25 under approval number K172073. 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 Hi-Torque Command 18 Guide Wire?

Hi-Torque Command 18 Guide Wire is a medical device that received FDA 510(k) clearance on 2017-08-25. It is manufactured by Abbott Vascular. The 510(k) number is K172073.

When was Hi-Torque Command 18 Guide Wire approved by the FDA?

Hi-Torque Command 18 Guide Wire received FDA 510(k) clearance on 2017-08-25, under approval number K172073.

What company makes Hi-Torque Command 18 Guide Wire?

Hi-Torque Command 18 Guide Wire is manufactured by Abbott Vascular.

What is the FDA product code for Hi-Torque Command 18 Guide Wire?

The FDA product code for Hi-Torque Command 18 Guide Wire 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.