FDA 510(k)

MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL

K-Number: K023084 · 2002-12-16

Decision Date2002-12-16

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Advances, Inc.. It received FDA 510(k) clearance on 2002-12-16 under 510(k) number K023084. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL?

MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL is a medical device that received FDA 510(k) clearance on 2002-12-16. The listed applicant is Medical Advances, Inc.. The 510(k) number is K023084.

When did MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL receive FDA 510(k) clearance?

MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL received FDA 510(k) clearance on 2002-12-16, under 510(k) number K023084.

Who is the listed applicant for MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL?

The FDA 510(k) record lists Medical Advances, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL?

The FDA product code for MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL is MOS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Advances, Inc. as applicant

K021433MODEL 415PH-64/42: PHASED ARRAY SHOULDER COIL K011608MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COIL K010074MODEL 455GE PHASED ARRAY WRIST COIL K003685MODEL 342GE-64 HIGH RESOLUTION BRAIN COIL K003144MODEL 205GE-64: PATHWAY MRI CAROTID ARRAY COIL K000345MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES

View all 57 devices →

Related Devices (Code: MOS)

K262330dS Breast 7ch 1.5TdS Breast 7ch 3.0TdS Breast 16ch 1.5TdS Breast 16ch 3.0TdS Breast Coil 7ch 1.5TdS Sentinelle Breast 16ch 1.5TdS Sentinelle Breast 16ch 3.0TPhilips Medical Systems Nederland B.V.K262294dS FootAnkle 16Ch 1.5T;dS FootAnkle 16Ch 3.0T;dS HiRes Hand/Wrist 16Ch 1.5T;dS HiRes Hand/Wrist 16CH 3.0T;dS Small Extremity 16Ch 1.5T;dS Small Extremity 16Ch 3.0TPhilips Medical Systems Nederland B.V.K2609470.55T 12Ch Breast CoilNeocoil, LLC K252587HD 8Ch Wrist ArrayShenzhen RF Tech Co., Ltd.K252876GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive OnlyShenzhen RF Tech Co., Ltd.K260519Smart Fit TorsoCardiac 1.5TPhilips Healthcare (Suzhou) Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.