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FDA 510(k)

TRULINE REINFORCED VALVED INFUSION CATHETER

K-Number: K021139 · 2002-04-17

ApplicantMicro Therapeutics, Inc.
Decision Date2002-04-17
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRULINE REINFORCED VALVED INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Micro Therapeutics, Inc.. It received FDA 510(k) clearance on 2002-04-17 under 510(k) number K021139. 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 TRULINE REINFORCED VALVED INFUSION CATHETER?

TRULINE REINFORCED VALVED INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 2002-04-17. The listed applicant is Micro Therapeutics, Inc.. The 510(k) number is K021139.

When did TRULINE REINFORCED VALVED INFUSION CATHETER receive FDA 510(k) clearance?

TRULINE REINFORCED VALVED INFUSION CATHETER received FDA 510(k) clearance on 2002-04-17, under 510(k) number K021139.

Who is the listed applicant for TRULINE REINFORCED VALVED INFUSION CATHETER?

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

What is the FDA product code for TRULINE REINFORCED VALVED INFUSION CATHETER?

The FDA product code for TRULINE REINFORCED VALVED INFUSION CATHETER is FOZ.

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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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