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FDA 510(k)

Symetrex Long Term Hemodialysis Catheter

K-Number: K171618 · 2017-11-16

Decision Date2017-11-16
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

Symetrex Long Term Hemodialysis Catheter is a medical device manufactured by Medcomp (Dba Medical Components, Inc.). It received FDA 510(k) clearance on 2017-11-16 under approval number K171618. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the Symetrex Long Term Hemodialysis Catheter?

Symetrex Long Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2017-11-16. It is manufactured by Medcomp (Dba Medical Components, Inc.). The 510(k) number is K171618.

When was Symetrex Long Term Hemodialysis Catheter approved by the FDA?

Symetrex Long Term Hemodialysis Catheter received FDA 510(k) clearance on 2017-11-16, under approval number K171618.

What company makes Symetrex Long Term Hemodialysis Catheter?

Symetrex Long Term Hemodialysis Catheter is manufactured by Medcomp (Dba Medical Components, Inc.).

What is the FDA product code for Symetrex Long Term Hemodialysis Catheter?

The FDA product code for Symetrex Long Term Hemodialysis Catheter is MSD.

Related Clinical Trials

Other Devices by Medcomp (Dba Medical Components, Inc.)

Related Devices (Code: MSD)

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.