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FDA 510(k)

MINI GHOST PTA CATHETER, MODEL 507

K-Number: K051343 · 2005-07-28

ApplicantNuMED, Inc.
Decision Date2005-07-28
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINI GHOST PTA CATHETER, MODEL 507 is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 2005-07-28 under 510(k) number K051343. 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 MINI GHOST PTA CATHETER, MODEL 507?

MINI GHOST PTA CATHETER, MODEL 507 is a medical device that received FDA 510(k) clearance on 2005-07-28. The listed applicant is NuMED, Inc.. The 510(k) number is K051343.

When did MINI GHOST PTA CATHETER, MODEL 507 receive FDA 510(k) clearance?

MINI GHOST PTA CATHETER, MODEL 507 received FDA 510(k) clearance on 2005-07-28, under 510(k) number K051343.

Who is the listed applicant for MINI GHOST PTA CATHETER, MODEL 507?

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 MINI GHOST PTA CATHETER, MODEL 507?

The FDA product code for MINI GHOST PTA CATHETER, MODEL 507 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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