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FDA 510(k)

NUMED MULLINS PTA CATHETER

K-Number: K013601 · 2002-01-03

ApplicantNuMED, Inc.
Decision Date2002-01-03
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NUMED MULLINS 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 2002-01-03 under 510(k) number K013601. 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 PTA CATHETER?

NUMED MULLINS PTA CATHETER is a medical device that received FDA 510(k) clearance on 2002-01-03. The listed applicant is NuMED, Inc.. The 510(k) number is K013601.

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

NUMED MULLINS PTA CATHETER received FDA 510(k) clearance on 2002-01-03, under 510(k) number K013601.

Who is the listed applicant for NUMED MULLINS 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 PTA CATHETER?

The FDA product code for NUMED MULLINS 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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