Vesco Medical Nasoenteric Feeding Tubes

FDA 510(k) K170162 · Vesco Medical, LLC

Substantially Equivalent

510(k) numberK170162

Submission

Device name
Vesco Medical Nasoenteric Feeding Tubes
Applicant
Vesco Medical, LLC
Columbus, OH, US
Received
January 18, 2017
Decision date
September 26, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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.

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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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K230326ENFit to ENFit Extension SetsPIF · Traditional 11/02/2023SE
K232205Vesco Q™ Enteral Feeding Pump; Vesco Q™ 500mL Bag Feed Set; Vesco Q™ 1000mL Bag Feed…LZH · Traditional 10/23/2023SE
K192991Vesco Medical Extension Feeding SetPIF · Traditional 08/03/2020SE
K170218Vesco Medical NRFit Tip SyringesFMF · Traditional 02/24/2017SE

Questions and answers

When was Vesco Medical Nasoenteric Feeding Tubes cleared by the FDA?

Vesco Medical Nasoenteric Feeding Tubes (K170162) received a 510(k) decision of Substantially Equivalent on September 26, 2017, 251 days after the submission was received.

What is the product code of K170162?

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