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FDA 510(k)

MULLINS-X, MODEL 250X

K-Number: K082868 · 2008-10-24

ApplicantNuMED, Inc.
Decision Date2008-10-24
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULLINS-X, MODEL 250X is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 2008-10-24 under 510(k) number K082868. 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 MULLINS-X, MODEL 250X?

MULLINS-X, MODEL 250X is a medical device that received FDA 510(k) clearance on 2008-10-24. The listed applicant is NuMED, Inc.. The 510(k) number is K082868.

When did MULLINS-X, MODEL 250X receive FDA 510(k) clearance?

MULLINS-X, MODEL 250X received FDA 510(k) clearance on 2008-10-24, under 510(k) number K082868.

Who is the listed applicant for MULLINS-X, MODEL 250X?

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 MULLINS-X, MODEL 250X?

The FDA product code for MULLINS-X, MODEL 250X 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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