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FDA 510(k)

NUMED MULLINS X PTA CATHETER

K-Number: K041093 · 2004-05-06

ApplicantNuMED, Inc.
Decision Date2004-05-06
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NUMED MULLINS X PTA CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 2004-05-06 under 510(k) number K041093. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUMED MULLINS X PTA CATHETER?

NUMED MULLINS X PTA CATHETER is a medical device that received FDA 510(k) clearance on 2004-05-06. The listed applicant is NuMED, Inc.. The 510(k) number is K041093.

When did NUMED MULLINS X PTA CATHETER receive FDA 510(k) clearance?

NUMED MULLINS X PTA CATHETER received FDA 510(k) clearance on 2004-05-06, under 510(k) number K041093.

Who is the listed applicant for NUMED MULLINS X PTA CATHETER?

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

What is the FDA product code for NUMED MULLINS X PTA CATHETER?

The FDA product code for NUMED MULLINS X PTA CATHETER is DQY.

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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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