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FDA 510(k)

NoCord

K-Number: K152826 · 2016-05-27

ApplicantCentrix, Inc.
Decision Date2016-05-27
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NoCord is a medical device manufactured by Centrix, Inc.. It received FDA 510(k) clearance on 2016-05-27 under approval number K152826. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NoCord?

NoCord is a medical device that received FDA 510(k) clearance on 2016-05-27. It is manufactured by Centrix, Inc.. The 510(k) number is K152826.

When was NoCord approved by the FDA?

NoCord received FDA 510(k) clearance on 2016-05-27, under approval number K152826.

What company makes NoCord?

NoCord is manufactured by Centrix, Inc..

What is the FDA product code for NoCord?

The FDA product code for NoCord is ELW.

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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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