Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MultiCross Catheter

K-Number: K152957 · 2016-03-04

Decision Date2016-03-04
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MultiCross Catheter is a medical device manufactured by Roxwood Medical, Inc.. It received FDA 510(k) clearance on 2016-03-04 under approval number K152957. 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 MultiCross Catheter?

MultiCross Catheter is a medical device that received FDA 510(k) clearance on 2016-03-04. It is manufactured by Roxwood Medical, Inc.. The 510(k) number is K152957.

When was MultiCross Catheter approved by the FDA?

MultiCross Catheter received FDA 510(k) clearance on 2016-03-04, under approval number K152957.

What company makes MultiCross Catheter?

MultiCross Catheter is manufactured by Roxwood Medical, Inc..

What is the FDA product code for MultiCross Catheter?

The FDA product code for MultiCross Catheter is DQY.

Other Devices by Roxwood Medical, Inc.

Related Devices (Code: DQY)

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.