8ch T/R Knee Coil

FDA 510(k) K223225 · Shenzhen RF Tech Co., Ltd.

Substantially Equivalent

510(k) numberK223225

Submission

Device name
8ch T/R Knee Coil
Applicant
Shenzhen RF Tech Co., Ltd.
Shenzhen, CN
Received
October 18, 2022
Decision date
February 14, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MOS – Coil, Magnetic Resonance, Specialty
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1000
Specialty
Radiology

Other 510(k)s with product code MOS

510(k)DeviceApplicantDecision
K262330dS Breast 7ch 1.5TdS Breast 7ch 3.0TdS Breast 16ch 1.5TdS Breast 16ch 3.0TdS Breast Coil…MOS · Special Philips Medical Systems Nederland B.V.07/30/2026SE
K262294dS FootAnkle 16Ch 1.5T;dS FootAnkle 16Ch 3.0T;dS HiRes Hand/Wrist 16Ch 1.5T;dS HiRes…MOS · Special Philips Medical Systems Nederland B.V.07/24/2026SE
K2609470.55T 12Ch Breast CoilMOS · Special Neocoil, LLC04/23/2026SE
K252587HD 8Ch Wrist ArrayMOS · Traditional Shenzhen RF Tech Co., Ltd.04/14/2026SE
K252876GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive…MOS · Traditional Shenzhen RF Tech Co., Ltd.04/01/2026SE
K260519Smart Fit TorsoCardiac 1.5TMOS · Special Philips Healthcare (Suzhou) Co., Ltd.03/20/2026SE
K252179GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive…MOS · Traditional Shenzhen RF Tech Co., Ltd.02/10/2026SE
K2537383.0T Air 32CH HnaMOS · Abbreviated Ge Healthcare Coils (Usa Instruments, Inc.)01/23/2026SE
K254190dS Base 1.5T; dS Base 3.0T; dS Head 1.5T; dS Head 3.0T; dS HeadNeck 1.5T; dS HeadNeck 3.0TMOS · Special Philips Medical Systems Nederland B.V.01/14/2026SE
K253182InkSpace Imaging Small Body Array (SBA12PH30x)MOS · Special Inkspace Imaging, Inc.10/20/2025SE

More from Inkspace Imaging, Inc.

510(k)DeviceDecision
K252587HD 8Ch Wrist ArrayMOS · Traditional 04/14/2026SE
K252876GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive…MOS · Traditional 04/01/2026SE
K252179GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive…MOS · Traditional 02/10/2026SE
K2310851.5T HD T/R Knee Array (10-F34127)MOS · Traditional 08/18/2023SE
K2232031.5T 24E Posterior ArrayLNH · Traditional 03/02/2023SE
K2232398ch Wrist CoilMOS · Traditional 12/08/2022SE
K2008368ch Flex SuiteMOS · Traditional 07/22/2020SE
K1722228ch Flex SuiteMOS · Traditional 12/08/2017SE
K1609328ch Foot Ankle CoilMOS · Traditional 08/01/2016SE
K1609358ch Foot Ankle CoilMOS · Traditional 07/28/2016SE

Questions and answers

When was 8ch T/R Knee Coil cleared by the FDA?

8ch T/R Knee Coil (K223225) received a 510(k) decision of Substantially Equivalent on February 14, 2023, 119 days after the submission was received.

What is the product code of K223225?

The FDA product code is MOS – Coil, Magnetic Resonance, Specialty, a Class II (moderate risk) device regulated under 21 CFR 892.1000.