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FDA 510(k)

Contour 24

K-Number: K173446 · 2017-11-17

ApplicantQuality Electrodynamics, LLC
Decision Date2017-11-17
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Contour 24 is the device name listed in this FDA 510(k) record. The listed applicant is Quality Electrodynamics, LLC. It received FDA 510(k) clearance on 2017-11-17 under 510(k) number K173446. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Contour 24?

Contour 24 is a medical device that received FDA 510(k) clearance on 2017-11-17. The listed applicant is Quality Electrodynamics, LLC. The 510(k) number is K173446.

When did Contour 24 receive FDA 510(k) clearance?

Contour 24 received FDA 510(k) clearance on 2017-11-17, under 510(k) number K173446.

Who is the listed applicant for Contour 24?

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

What is the FDA product code for Contour 24?

The FDA product code for Contour 24 is MOS.

Other records listing Quality Electrodynamics, LLC as applicant

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Related Devices (Code: MOS)

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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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