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FDA 510(k)

Rubicon 14, 18 and 35 Support Catheters

K-Number: K171913 · 2017-07-25

ApplicantBoston Scientific Corporation
Decision Date2017-07-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Rubicon 14, 18 and 35 Support Catheters is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2017-07-25 under approval number K171913. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Rubicon 14, 18 and 35 Support Catheters?

Rubicon 14, 18 and 35 Support Catheters is a medical device that received FDA 510(k) clearance on 2017-07-25. It is manufactured by Boston Scientific Corporation. The 510(k) number is K171913.

When was Rubicon 14, 18 and 35 Support Catheters approved by the FDA?

Rubicon 14, 18 and 35 Support Catheters received FDA 510(k) clearance on 2017-07-25, under approval number K171913.

What company makes Rubicon 14, 18 and 35 Support Catheters?

Rubicon 14, 18 and 35 Support Catheters is manufactured by Boston Scientific Corporation.

What is the FDA product code for Rubicon 14, 18 and 35 Support Catheters?

The FDA product code for Rubicon 14, 18 and 35 Support Catheters is DQY.

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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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