Enteral Transition Adaptor— 510(k) K220165

Substantially Equivalent

GBUK Group, Ltd.

FDA 510(k) clearance K220165 for Enteral Transition Adaptor, Substantially Equivalent on 2022-10-21. Applicant: GBUK Group, Ltd.. Device class: 2.

Clearance details

Applicant: GBUK Group, Ltd.
Product code: Code PIO
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 2022-01-20
Decision date: 2022-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Selby, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.