FDA 510(k)

Upstream GoBack Crossing Catheter

K-Number: K182937 · 2019-05-23

ApplicantUpstream Peripheral Technologies, Ltd.

Decision Date2019-05-23

Product CodeDQY

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Upstream GoBack Crossing Catheter is a medical device manufactured by Upstream Peripheral Technologies, Ltd.. It received FDA 510(k) clearance on 2019-05-23 under approval number K182937. 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 Upstream GoBack Crossing Catheter?

Upstream GoBack Crossing Catheter is a medical device that received FDA 510(k) clearance on 2019-05-23. It is manufactured by Upstream Peripheral Technologies, Ltd.. The 510(k) number is K182937.

When was Upstream GoBack Crossing Catheter approved by the FDA?

Upstream GoBack Crossing Catheter received FDA 510(k) clearance on 2019-05-23, under approval number K182937.

What company makes Upstream GoBack Crossing Catheter?

Upstream GoBack Crossing Catheter is manufactured by Upstream Peripheral Technologies, Ltd..

What is the FDA product code for Upstream GoBack Crossing Catheter?

The FDA product code for Upstream GoBack Crossing Catheter is DQY.

Other Devices by Upstream Peripheral Technologies, Ltd.

K211802GoBack Crossing Catheter

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.