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FDA 510(k)

MEDRAD QUADRATURE CTL ARRAY COIL

K-Number: K984159 · 1999-01-12

ApplicantMedrad, Inc.
Decision Date1999-01-12
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDRAD QUADRATURE CTL ARRAY COIL is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1999-01-12 under 510(k) number K984159. 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 MEDRAD QUADRATURE CTL ARRAY COIL?

MEDRAD QUADRATURE CTL ARRAY COIL is a medical device that received FDA 510(k) clearance on 1999-01-12. The listed applicant is Medrad, Inc.. The 510(k) number is K984159.

When did MEDRAD QUADRATURE CTL ARRAY COIL receive FDA 510(k) clearance?

MEDRAD QUADRATURE CTL ARRAY COIL received FDA 510(k) clearance on 1999-01-12, under 510(k) number K984159.

Who is the listed applicant for MEDRAD QUADRATURE CTL ARRAY COIL?

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

What is the FDA product code for MEDRAD QUADRATURE CTL ARRAY COIL?

The FDA product code for MEDRAD QUADRATURE CTL ARRAY COIL is MOS.

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Related Devices (Code: MOS)

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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, LLCK252587HD 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.

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