Sentinelle Endo Coil Array for Pelvic Imaging

FDA 510(k) K103274 · Sentinelle Medical, Inc.

Substantially Equivalent

510(k) numberK103274

Submission

Device name
Sentinelle Endo Coil Array for Pelvic Imaging
Applicant
Sentinelle Medical, Inc.
Toronto, Ontario, CA
Received
November 5, 2010
Decision date
August 18, 2011
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
K100113Vanguard Breast MRI Auxiliary Table with 16 Channel Coil Array for GE 3T MRI System…MOS · Special 04/22/2010SE
K093672Aegis Navigation Anda Egis Pelvic ApplicationLLZ · Traditional 12/11/2009SE
K070244AegisLLZ · Traditional 02/09/2007SE
K060873Vanguard MRI Auxiliary Patient Table with 4 and 8 Channel Coil Array for GE Signa SystemsMOS · Traditional 04/14/2006SE

Questions and answers

When was Sentinelle Endo Coil Array for Pelvic Imaging cleared by the FDA?

Sentinelle Endo Coil Array for Pelvic Imaging (K103274) received a 510(k) decision of Substantially Equivalent on August 18, 2011, 286 days after the submission was received.

What is the product code of K103274?

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