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FDA 510(k)

MEDX HOME

K-Number: K050022 · 2005-05-05

ApplicantMedx Electronics, Inc.
Decision Date2005-05-05
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDX HOME is the device name listed in this FDA 510(k) record. The listed applicant is Medx Electronics, Inc.. It received FDA 510(k) clearance on 2005-05-05 under 510(k) number K050022. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDX HOME?

MEDX HOME is a medical device that received FDA 510(k) clearance on 2005-05-05. The listed applicant is Medx Electronics, Inc.. The 510(k) number is K050022.

When did MEDX HOME receive FDA 510(k) clearance?

MEDX HOME received FDA 510(k) clearance on 2005-05-05, under 510(k) number K050022.

Who is the listed applicant for MEDX HOME?

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

What is the FDA product code for MEDX HOME?

The FDA product code for MEDX HOME is ILY.

Other records listing Medx Electronics, Inc. as applicant

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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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