1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil

FDA 510(k) K222257 · Invivo Corporation (Business Trade Name: Philips)

Substantially Equivalent

510(k) numberK222257

Submission

Device name
1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil
Applicant
Invivo Corporation (Business Trade Name: Philips)
Florida, FL, US
Received
July 27, 2022
Decision date
August 23, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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
K232762dS Breast Coil 7ch 1.5TMOS · Special 10/03/2023SE
K2223258ch Wrist CoilMOS · Traditional 08/31/2022SE
K213735dS Sentinelle Breast 16ch 1.5T CoilMOS · Traditional 08/08/2022SE
K213727dS Sentinelle Breast 16ch 3.0T CoilMOS · Traditional 08/08/2022SE
K213351ds Head 32ch 3.0TMOS · Traditional 10/29/2021SE

Questions and answers

When was 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil cleared by the FDA?

1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil (K222257) received a 510(k) decision of Substantially Equivalent on August 23, 2022, 27 days after the submission was received.

What is the product code of K222257?

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