Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Cair Lgl. It received FDA 510(k) clearance on 2024-01-22 under 510(k) 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. The listed applicant is Cair Lgl. The 510(k) number is K231299.

When did Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector receive FDA 510(k) clearance?

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

Who is the listed applicant for Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector?

The FDA 510(k) record lists Cair Lgl as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Cair Lgl 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.

View all 7 devices →

Related Devices (Code: PIO)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.