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FDA 510(k)

FFR V2.5

K-Number: K170133 · 2017-05-26

ApplicantPhilips Volcano
Decision Date2017-05-26
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FFR V2.5 is a medical device manufactured by Philips Volcano. It received FDA 510(k) clearance on 2017-05-26 under approval number K170133. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FFR V2.5?

FFR V2.5 is a medical device that received FDA 510(k) clearance on 2017-05-26. It is manufactured by Philips Volcano. The 510(k) number is K170133.

When was FFR V2.5 approved by the FDA?

FFR V2.5 received FDA 510(k) clearance on 2017-05-26, under approval number K170133.

What company makes FFR V2.5?

FFR V2.5 is manufactured by Philips Volcano.

What is the FDA product code for FFR V2.5?

The FDA product code for FFR V2.5 is IYO.

Other Devices by Philips Volcano

K162418Pioneer Plus Catheter

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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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