Glidewire GT
K-Number: K170417 · 2017-09-15
ApplicantTerumo Corporation
Decision Date2017-09-15
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Glidewire GT is a medical device manufactured by Terumo Corporation. It received FDA 510(k) clearance on 2017-09-15 under approval number K170417. 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 Glidewire GT?
Glidewire GT is a medical device that received FDA 510(k) clearance on 2017-09-15. It is manufactured by Terumo Corporation. The 510(k) number is K170417.
When was Glidewire GT approved by the FDA?
Glidewire GT received FDA 510(k) clearance on 2017-09-15, under approval number K170417.
What company makes Glidewire GT?
Glidewire GT is manufactured by Terumo Corporation.
What is the FDA product code for Glidewire GT?
The FDA product code for Glidewire GT 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.