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)

Critical Care Suite with Enteric Tube Positioning AI Algorithm

K-Number: K253502 · 2026-04-14

Decision Date2026-04-14
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Critical Care Suite with Enteric Tube Positioning AI Algorithm is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems, LLC. It received FDA 510(k) clearance on 2026-04-14 under 510(k) number K253502. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Critical Care Suite with Enteric Tube Positioning AI Algorithm?

Critical Care Suite with Enteric Tube Positioning AI Algorithm is a medical device that received FDA 510(k) clearance on 2026-04-14. The listed applicant is Ge Medical Systems, LLC. The 510(k) number is K253502.

When did Critical Care Suite with Enteric Tube Positioning AI Algorithm receive FDA 510(k) clearance?

Critical Care Suite with Enteric Tube Positioning AI Algorithm received FDA 510(k) clearance on 2026-04-14, under 510(k) number K253502.

Who is the listed applicant for Critical Care Suite with Enteric Tube Positioning AI Algorithm?

The FDA 510(k) record lists Ge Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Critical Care Suite with Enteric Tube Positioning AI Algorithm?

The FDA product code for Critical Care Suite with Enteric Tube Positioning AI Algorithm is QIH.

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 Ge Medical Systems, LLC 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 47 devices →

Related Devices (Code: QIH)

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.