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FDA 510(k)

ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER

K-Number: K900263 · 1990-07-24

ApplicantArrow Intl., Inc.
Decision Date1990-07-24
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1990-07-24 under 510(k) number K900263. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER?

ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1990-07-24. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K900263.

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

ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1990-07-24, under 510(k) number K900263.

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

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

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

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

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: FOZ)

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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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