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FDA 510(k)

Luminoah FLOW™ Enteral Nutrition System

K-Number: K253558 · 2026-04-20

ApplicantLuminoah
Decision Date2026-04-20
Product CodeLZH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Luminoah FLOW™ Enteral Nutrition System is the device name listed in this FDA 510(k) record. The listed applicant is Luminoah. It received FDA 510(k) clearance on 2026-04-20 under 510(k) number K253558. The device is classified under product code LZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Luminoah FLOW™ Enteral Nutrition System?

Luminoah FLOW™ Enteral Nutrition System is a medical device that received FDA 510(k) clearance on 2026-04-20. The listed applicant is Luminoah. The 510(k) number is K253558.

When did Luminoah FLOW™ Enteral Nutrition System receive FDA 510(k) clearance?

Luminoah FLOW™ Enteral Nutrition System received FDA 510(k) clearance on 2026-04-20, under 510(k) number K253558.

Who is the listed applicant for Luminoah FLOW™ Enteral Nutrition System?

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

What is the FDA product code for Luminoah FLOW™ Enteral Nutrition System?

The FDA product code for Luminoah FLOW™ Enteral Nutrition System is LZH.

Related Devices (Code: LZH)

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.