Proton Positioing and Immobilization Devices

FDA 510(k) K180021 · Medtec Inc Dba Civco Medical Solutions and Civco Radiotherap

Substantially Equivalent

510(k) numberK180021

Submission

Device name
Proton Positioing and Immobilization Devices
Applicant
Medtec Inc Dba Civco Medical Solutions and Civco Radiotherap
Orange City, IA, US
Received
January 3, 2018
Decision date
June 29, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IYE – Accelerator, Linear, Medical
Device class
Class II (moderate risk)
Regulation
21 CFR 892.5050
Specialty
Radiology

Other 510(k)s with product code IYE

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K261718EZFluence (RADEZ V2)IYE · Traditional Radformation, Inc.08/31/2026SE
K260733MRIA Radiation Therapy Information System (MRIA)IYE · Traditional Manteia Technologies Co., Ltd.08/26/2026SE
K261856Halcyon, Ethos Radiotherapy System (5.0)IYE · Traditional Varian Medical Systems, Inc.08/03/2026SE
K252937ThinkQA 3IYE · Traditional Dosisoft SA06/12/2026SE
K253004Luna 3DIYE · Traditional Lap GmbH Laser Applikationen06/04/2026SE
K260792AerFrame Patient Immobilization System (AFPIS)IYE · Traditional Stabilix, LLC05/08/2026SE
K252258Veriqa RT Epid 3DIYE · Traditional Ptw-Freiburg Physikalisch-Technische-Werkstaetten…04/15/2026SE
K253962ClearCheck (RADCC V2.7)IYE · Traditional Radformation, Inc.04/03/2026SE
K253012AlignRT Plus (8.0)IYE · Traditional Vision Rt, Ltd.03/18/2026SE
K252977Halcyon, Ethos Radiotherapy System (5.0)IYE · Traditional Varian Medical Systems, Inc.01/21/2026SE

Questions and answers

When was Proton Positioing and Immobilization Devices cleared by the FDA?

Proton Positioing and Immobilization Devices (K180021) received a 510(k) decision of Substantially Equivalent on June 29, 2018, 177 days after the submission was received.

What is the product code of K180021?

The FDA product code is IYE – Accelerator, Linear, Medical, a Class II (moderate risk) device regulated under 21 CFR 892.5050.