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FDA 510(k)

CARESTATION 126S VIDEOPHONE

K-Number: K031863 · 2003-10-10

ApplicantMotion Media Technology, Inc.
Decision Date2003-10-10
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARESTATION 126S VIDEOPHONE is the device name listed in this FDA 510(k) record. The listed applicant is Motion Media Technology, Inc.. It received FDA 510(k) clearance on 2003-10-10 under 510(k) number K031863. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARESTATION 126S VIDEOPHONE?

CARESTATION 126S VIDEOPHONE is a medical device that received FDA 510(k) clearance on 2003-10-10. The listed applicant is Motion Media Technology, Inc.. The 510(k) number is K031863.

When did CARESTATION 126S VIDEOPHONE receive FDA 510(k) clearance?

CARESTATION 126S VIDEOPHONE received FDA 510(k) clearance on 2003-10-10, under 510(k) number K031863.

Who is the listed applicant for CARESTATION 126S VIDEOPHONE?

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

What is the FDA product code for CARESTATION 126S VIDEOPHONE?

The FDA product code for CARESTATION 126S VIDEOPHONE is MWI.

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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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