ST Sense NV 8 Array Coil

FDA 510(k) K140282 · Resonance Innovations, LLC

Substantially Equivalent

510(k) numberK140282

Submission

Device name
ST Sense NV 8 Array Coil
Applicant
Resonance Innovations, LLC
Omaha, NE, US
Received
February 4, 2014
Decision date
February 26, 2014
Decision
Substantially Equivalent (SESE)
Type
Special 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

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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.

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K142676Siemens 3.0T PROCURE Array CoilMOS · Special 12/05/2014SE
K142755Siemens 3.0 Blanket Array CoilMOS · Traditional 10/23/2014SE
K1406061.5T Procure Array Coil, 3.0T Procure Array CoilMOS · Special 05/12/2014SE
K1339861.5T Orbit and Mandible Array, 3.0T Orbit and Mandible ArrayMOS · Traditional 01/27/2014SE
K1304573T Distal Coil, 3T Elbow Coil, 3T Long Bone CoilMOS · Special 05/20/2013SE
K0611703.0T Pediatric Head and Spine Array, Model 808GE3000MOS · Special 05/25/2006SE
K0606891.5T Pediatric Head and Spine Array ModelMOS · Special 03/31/2006SE

Questions and answers

When was ST Sense NV 8 Array Coil cleared by the FDA?

ST Sense NV 8 Array Coil (K140282) received a 510(k) decision of Substantially Equivalent on February 26, 2014, 22 days after the submission was received.

What is the product code of K140282?

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