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FDA 510(k)

CenterCross Ultra LV Catheter

K-Number: K170403 · 2017-03-07

ApplicantRoxwood Medical, Inc.
Decision Date2017-03-07
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CenterCross Ultra LV Catheter is a medical device manufactured by Roxwood Medical, Inc.. It received FDA 510(k) clearance on 2017-03-07 under approval number K170403. 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 CenterCross Ultra LV Catheter?

CenterCross Ultra LV Catheter is a medical device that received FDA 510(k) clearance on 2017-03-07. It is manufactured by Roxwood Medical, Inc.. The 510(k) number is K170403.

When was CenterCross Ultra LV Catheter approved by the FDA?

CenterCross Ultra LV Catheter received FDA 510(k) clearance on 2017-03-07, under approval number K170403.

What company makes CenterCross Ultra LV Catheter?

CenterCross Ultra LV Catheter is manufactured by Roxwood Medical, Inc..

What is the FDA product code for CenterCross Ultra LV Catheter?

The FDA product code for CenterCross Ultra LV Catheter is DQY.

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Other Devices by Roxwood Medical, Inc.

K160681CenterCross Ultra Catheter K152957MultiCross Catheter K152456CenterCross Ultra 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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