Enteral Extension Sets

FDA 510(k) K203633 · GBUK Group, Ltd.

Substantially Equivalent

510(k) numberK203633

Submission

Device name
Enteral Extension Sets
Applicant
GBUK Group, Ltd.
Selby, GB
Received
December 11, 2020
Decision date
August 19, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
PIF – Gastrointestinal Tubes With Enteral Specific Connectors
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

To facilitate enteral specific connections.

Other 510(k)s with product code PIF

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K260110danumed Extension Set for Gastrostomy ButtonPIF · Traditional Danumed Medizintechnik GmbH09/10/2026SE
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K254170Percutaneous Endoscopic Gastrostomy (PEG) KitPIF · Traditional Degania Silicone , Ltd.03/20/2026SE
K242917Enteral Drainage System, Enteral Medicine strawPIF · Traditional HMC Premedical S.p.A.06/18/2025SE
K250481Extension Feeding Set with ENFit™ ConnectorsPIF · Traditional SKY Medical, a.s.04/18/2025SE
K240052Disposable Enteral Feeding SetsPIF · Traditional Beijing L&Z Medical Technology Development Co.…07/03/2024SE
K233034Mobility+ Enteral Feeding System OTCPIF · Traditional Rockfield Medical04/12/2024SE
K230326ENFit to ENFit Extension SetsPIF · Traditional Vesco Medical11/02/2023SE
K232046Kangaroo Skin Level Balloon Gastrostomy Kit, Kangaroo Bolus Feed Set with ENFIT…PIF · Traditional Xeridiem Medical Devices, A Spectrum Plastics…10/06/2023SE
K222773Feeding TubePIF · Traditional Anhui Tiankang Medical Technology Co., Ltd.08/17/2023SE

More from Anhui Tiankang Medical Technology Co., Ltd.

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Questions and answers

When was Enteral Extension Sets cleared by the FDA?

Enteral Extension Sets (K203633) received a 510(k) decision of Substantially Equivalent on August 19, 2021, 251 days after the submission was received.

What is the product code of K203633?

The FDA product code is PIF – Gastrointestinal Tubes With Enteral Specific Connectors, a Class II (moderate risk) device regulated under 21 CFR 876.5980.