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FDA 510(k)

Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector

K-Number: K231299 · 2024-01-22

ApplicantCair Lgl
Decision Date2024-01-22
Product CodePIO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector is a medical device manufactured by Cair Lgl. It received FDA 510(k) clearance on 2024-01-22 under approval number K231299. The device is classified under product code PIO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector?

Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector is a medical device that received FDA 510(k) clearance on 2024-01-22. It is manufactured by Cair Lgl. The 510(k) number is K231299.

When was Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector approved by the FDA?

Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector received FDA 510(k) clearance on 2024-01-22, under approval number K231299.

What company makes Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector?

Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector is manufactured by Cair Lgl.

What is the FDA product code for Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector?

The FDA product code for Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector is PIO.

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Related Devices (Code: PIO)

K151237Nutrisafe 2- ENFit AdaptorVygon K162254Cedic Enteral ENFit Transition ConnectorsCedic S.R.L. K220165Enteral Transition AdaptorGBUK Group, Ltd. K233190ENFit AdaptorJiangsu Caina Medical Co.,Ltd

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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