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FDA 510(k)

MDXNET

K-Number: K060035 · 2006-03-09

ApplicantCybermdx, Inc.
Decision Date2006-03-09
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MDXNET is the device name listed in this FDA 510(k) record. The listed applicant is Cybermdx, Inc.. It received FDA 510(k) clearance on 2006-03-09 under 510(k) number K060035. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDXNET?

MDXNET is a medical device that received FDA 510(k) clearance on 2006-03-09. The listed applicant is Cybermdx, Inc.. The 510(k) number is K060035.

When did MDXNET receive FDA 510(k) clearance?

MDXNET received FDA 510(k) clearance on 2006-03-09, under 510(k) number K060035.

Who is the listed applicant for MDXNET?

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

What is the FDA product code for MDXNET?

The FDA product code for MDXNET is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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