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FDA 510(k)

FENESTRATED INFUSION CATHETER

K-Number: K024190 · 2003-03-17

ApplicantPromedic, Inc.
Decision Date2003-03-17
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FENESTRATED INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Promedic, Inc.. It received FDA 510(k) clearance on 2003-03-17 under 510(k) number K024190. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FENESTRATED INFUSION CATHETER?

FENESTRATED INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 2003-03-17. The listed applicant is Promedic, Inc.. The 510(k) number is K024190.

When did FENESTRATED INFUSION CATHETER receive FDA 510(k) clearance?

FENESTRATED INFUSION CATHETER received FDA 510(k) clearance on 2003-03-17, under 510(k) number K024190.

Who is the listed applicant for FENESTRATED INFUSION CATHETER?

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

What is the FDA product code for FENESTRATED INFUSION CATHETER?

The FDA product code for FENESTRATED INFUSION CATHETER is FRN.

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Other records listing Promedic, Inc. as applicant

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Related Devices (Code: FRN)

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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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