31P/1H Dual Tuned Surface Coil 3T; 23NA/ 1H Dual Turned Surface Coil 3T; 13C /1H Dual Turned Surface Coil 3T

FDA 510(k) K102348 · Rapid Biomedical GmbH

Substantially Equivalent

510(k) numberK102348

Submission

Device name
31P/1H Dual Tuned Surface Coil 3T; 23NA/ 1H Dual Turned Surface Coil 3T; 13C /1H Dual Turned Surface Coil 3T
Applicant
Rapid Biomedical GmbH
Rimpar, Bavaria, DE
Received
August 19, 2010
Decision date
December 22, 2010
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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
K21348031P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head CoilMOS · Traditional 02/01/2023SE
K1915391.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil SupportMOS · Traditional 01/31/2020SE
K1819481.5T 16Ch Diagnostic Breast Coil, 3.0T 16Ch Diagnostic Breast CoilMOS · Traditional 11/16/2018SE
K163661P-140-Flex Coil, Na-140-Flex Coil, C-140-Flex CoilMOS · Traditional 03/21/2018SE
K10274831P/1H Head Coil 3T; 23NA/1H Head Coil 3T; 13C/1H Head Coil 3TMOS · Abbreviated 05/13/2011SE
K08325516CH Ai Breast Coils 1.5 T and 3 TMOS · Traditional 11/21/2008SE

Questions and answers

When was 31P/1H Dual Tuned Surface Coil 3T; 23NA/ 1H Dual Turned Surface Coil 3T; 13C /1H Dual Turned Surface Coil 3T cleared by the FDA?

31P/1H Dual Tuned Surface Coil 3T; 23NA/ 1H Dual Turned Surface Coil 3T; 13C /1H Dual Turned Surface Coil 3T (K102348) received a 510(k) decision of Substantially Equivalent on December 22, 2010, 125 days after the submission was received.

What is the product code of K102348?

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