Verrata PLUS Pressure Guide Wire
K-Number: K210235 · 2021-04-15
ApplicantVolcano Corporation
Decision Date2021-04-15
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Verrata PLUS Pressure Guide Wire is a medical device manufactured by Volcano Corporation. It received FDA 510(k) clearance on 2021-04-15 under approval number K210235. 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 Verrata PLUS Pressure Guide Wire?
Verrata PLUS Pressure Guide Wire is a medical device that received FDA 510(k) clearance on 2021-04-15. It is manufactured by Volcano Corporation. The 510(k) number is K210235.
When was Verrata PLUS Pressure Guide Wire approved by the FDA?
Verrata PLUS Pressure Guide Wire received FDA 510(k) clearance on 2021-04-15, under approval number K210235.
What company makes Verrata PLUS Pressure Guide Wire?
Verrata PLUS Pressure Guide Wire is manufactured by Volcano Corporation.
What is the FDA product code for Verrata PLUS Pressure Guide Wire?
The FDA product code for Verrata PLUS Pressure 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.