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FDA 510(k)

Entuit PEG, Entuit PEGJ

K-Number: K183336 · 2019-05-29

ApplicantWilson-Cook Medical, Inc.
Decision Date2019-05-29
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

Entuit PEG, Entuit PEGJ is a medical device manufactured by Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2019-05-29 under approval number K183336. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the Entuit PEG, Entuit PEGJ?

Entuit PEG, Entuit PEGJ is a medical device that received FDA 510(k) clearance on 2019-05-29. It is manufactured by Wilson-Cook Medical, Inc.. The 510(k) number is K183336.

When was Entuit PEG, Entuit PEGJ approved by the FDA?

Entuit PEG, Entuit PEGJ received FDA 510(k) clearance on 2019-05-29, under approval number K183336.

What company makes Entuit PEG, Entuit PEGJ?

Entuit PEG, Entuit PEGJ is manufactured by Wilson-Cook Medical, Inc..

What is the FDA product code for Entuit PEG, Entuit PEGJ?

The FDA product code for Entuit PEG, Entuit PEGJ is KNT.

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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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