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FDA 510(k)

ARGON DUAL LUMEN HEMODIALYSIS, CATHETER

K-Number: K842039 · 1985-01-29

ApplicantArgon Medical Corp.
Decision Date1985-01-29
Product CodeKNZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGON DUAL LUMEN HEMODIALYSIS, CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1985-01-29 under 510(k) number K842039. The device is classified under product code KNZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGON DUAL LUMEN HEMODIALYSIS, CATHETER?

ARGON DUAL LUMEN HEMODIALYSIS, CATHETER is a medical device that received FDA 510(k) clearance on 1985-01-29. The listed applicant is Argon Medical Corp.. The 510(k) number is K842039.

When did ARGON DUAL LUMEN HEMODIALYSIS, CATHETER receive FDA 510(k) clearance?

ARGON DUAL LUMEN HEMODIALYSIS, CATHETER received FDA 510(k) clearance on 1985-01-29, under 510(k) number K842039.

Who is the listed applicant for ARGON DUAL LUMEN HEMODIALYSIS, CATHETER?

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

What is the FDA product code for ARGON DUAL LUMEN HEMODIALYSIS, CATHETER?

The FDA product code for ARGON DUAL LUMEN HEMODIALYSIS, CATHETER is KNZ.

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Other records listing Argon Medical Corp. as applicant

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Related Devices (Code: KNZ)

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.

K844612ACUTE HEMODIALYSIS TRAYSPackaging Technologies, Inc.K842864VACCESS FEMORAL CANNULAVas-Cath of Canada , Ltd.K842416DUO FLOW CATHETER-MC 54Medical Components, Inc.K841530DOUBLE LUMEN SUBLCAVIAN-FEMORALMedical Components, Inc.K841119TOPS DISPOS. INFUSION SET/HEMODIALYSISTop Surgical Manufacturers Co.K840424HEMOCATH REPAIR KITQuinton, 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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