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FDA 510(k)

Trio-CT­® Triple Lumen Catheter w/ Curved Extensions

K-Number: K232945 · 2023-11-16

Decision Date2023-11-16
Product CodeNIE
Advisory CommitteeGU
DecisionUnknown

Device Summary

Trio-CT­® Triple Lumen Catheter w/ Curved Extensions is a medical device manufactured by Medical Components, Inc. (dba MedComp). It received FDA 510(k) clearance on 2023-11-16 under approval number K232945. The device is classified under product code NIE. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

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

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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.