Trio-CT® Triple Lumen Catheter w/ Curved Extensions
K-Number: K232945 · 2023-11-16
Device Summary
Frequently Asked Questions
What is the Trio-CT® Triple Lumen Catheter w/ Curved Extensions?
Trio-CT® Triple Lumen Catheter w/ Curved Extensions is a medical device that received FDA 510(k) clearance on 2023-11-16. It is manufactured by Medical Components, Inc. (dba MedComp). The 510(k) number is K232945.
When was Trio-CT® Triple Lumen Catheter w/ Curved Extensions approved by the FDA?
Trio-CT® Triple Lumen Catheter w/ Curved Extensions received FDA 510(k) clearance on 2023-11-16, under approval number K232945.
What company makes Trio-CT® Triple Lumen Catheter w/ Curved Extensions?
Trio-CT® Triple Lumen Catheter w/ Curved Extensions is manufactured by Medical Components, Inc. (dba MedComp).
What is the FDA product code for Trio-CT® Triple Lumen Catheter w/ Curved Extensions?
The FDA product code for Trio-CT® Triple Lumen Catheter w/ Curved Extensions is NIE.
Related Clinical Trials
Other Devices by Medical Components, Inc. (dba MedComp)
Related Devices (Code: NIE)
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.