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FDA 510(k)

ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER

K-Number: K984189 · 1999-05-05

ApplicantMaxxim Medical
Decision Date1999-05-05
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Maxxim Medical. It received FDA 510(k) clearance on 1999-05-05 under 510(k) number K984189. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER?

ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1999-05-05. The listed applicant is Maxxim Medical. The 510(k) number is K984189.

When did ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1999-05-05, under 510(k) number K984189.

Who is the listed applicant for ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER?

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

What is the FDA product code for ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER?

The FDA product code for ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER is FOZ.

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Other records listing Maxxim Medical as applicant

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Related Devices (Code: FOZ)

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.

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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.

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