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FDA 510(k)

Nasogastric Feeding Tubes - ENFit Port - PVC

K-Number: K213258 · 2022-06-09

ApplicantCair Lgl
Decision Date2022-06-09
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Nasogastric Feeding Tubes - ENFit Port - PVC is the device name listed in this FDA 510(k) record. The listed applicant is Cair Lgl. It received FDA 510(k) clearance on 2022-06-09 under 510(k) number K213258. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nasogastric Feeding Tubes - ENFit Port - PVC?

Nasogastric Feeding Tubes - ENFit Port - PVC is a medical device that received FDA 510(k) clearance on 2022-06-09. The listed applicant is Cair Lgl. The 510(k) number is K213258.

When did Nasogastric Feeding Tubes - ENFit Port - PVC receive FDA 510(k) clearance?

Nasogastric Feeding Tubes - ENFit Port - PVC received FDA 510(k) clearance on 2022-06-09, under 510(k) number K213258.

Who is the listed applicant for Nasogastric Feeding Tubes - ENFit Port - PVC?

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 Nasogastric Feeding Tubes - ENFit Port - PVC?

The FDA product code for Nasogastric Feeding Tubes - ENFit Port - PVC is PIF.

Related Clinical Trials

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.

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: PIF)

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.