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FDA 510(k)

Entuit PEG, Entuit PEGJ

K-Number: K183336 · 2019-05-29

Decision Date2019-05-29
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

Entuit PEG, Entuit PEGJ is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2019-05-29 under 510(k) 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. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K183336.

When did Entuit PEG, Entuit PEGJ receive FDA 510(k) clearance?

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

Who is the listed applicant for Entuit PEG, Entuit PEGJ?

The FDA 510(k) record lists Wilson-Cook Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Wilson-Cook Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KNT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.