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FDA 510(k)

MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER

K-Number: K012562 · 2002-02-08

ApplicantMedical Components, Inc.
Decision Date2002-02-08
Product CodeMSD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 2002-02-08 under 510(k) number K012562. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER?

MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 2002-02-08. The listed applicant is Medical Components, Inc.. The 510(k) number is K012562.

When did MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER receive FDA 510(k) clearance?

MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER received FDA 510(k) clearance on 2002-02-08, under 510(k) number K012562.

Who is the listed applicant for MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER?

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

What is the FDA product code for MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER?

The FDA product code for MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER is MSD.

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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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