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FDA 510(k)

Symetrex Long Term Hemodialysis Catheter

K-Number: K171618 · 2017-11-16

ApplicantMedcomp (Dba Medical Components, Inc.)
Decision Date2017-11-16
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

Symetrex Long Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp (Dba Medical Components, Inc.). It received FDA 510(k) clearance on 2017-11-16 under 510(k) 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. The listed applicant is Medcomp (Dba Medical Components, Inc.). The 510(k) number is K171618.

When did Symetrex Long Term Hemodialysis Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Symetrex Long Term Hemodialysis Catheter?

The FDA 510(k) record lists Medcomp (Dba Medical Components, Inc.) as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Medcomp (Dba Medical Components, Inc.) as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K171483ArchFlo CT MidlineK17133320G x 5/8 Pro-Lock CT Safety Infusion Set

Related Devices (Code: MSD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241581Hemodialysis CatheterHaolang Medical USA CorporationK210461End CapMedical Components Inc (Medcomp)K203575GlidePath Retro Long-Term Hemodialysis CatheterC.R. Bard, Inc.K211410GlidePath 13F Long-Term Hemodialysis CatheterBard Peripheral Vascular, Inc.K203767Pristine Long-Term Hemodialysis CatheterC B Bard, Inc.K202150GlidePath 7.5F Long-Term Dialysis CatheterC.R. Bard, Inc.

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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