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FDA 510(k)

PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL

K-Number: K932091 · 1993-12-14

ApplicantMagnetic Research, Inc.
Decision Date1993-12-14
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL is the device name listed in this FDA 510(k) record. The listed applicant is Magnetic Research, Inc.. It received FDA 510(k) clearance on 1993-12-14 under 510(k) number K932091. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL?

PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL is a medical device that received FDA 510(k) clearance on 1993-12-14. The listed applicant is Magnetic Research, Inc.. The 510(k) number is K932091.

When did PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL receive FDA 510(k) clearance?

PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL received FDA 510(k) clearance on 1993-12-14, under 510(k) number K932091.

Who is the listed applicant for PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL?

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

What is the FDA product code for PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL?

The FDA product code for PHASED ARRAY/BILATERAL QUADRATURE CONTOUR COIL is LNH.

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Other records listing Magnetic Research, Inc. as applicant

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.

K935015QUADRATURE SMALL EXTREMITY COILK932552SPORTS MEDICINE QUADRATURE SHOULDER COILK931795TELERAD STATK930991BILATERAL TEMPORAL MANDIBULAR JOINT COILK923881QUADRATURE CERVICAL CONTOUR COILK920227QUADRATURE SHOULDER CONTOUR COIL

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Related Devices (Code: LNH)

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K261758Embrace Vision Neonatal MRI SystemAspect Imaging, Ltd.K261283APERTO Lucent MRI SystemFujifilm CorporationK260758MAGNETOM Free.Max; MAGNETOM Free.StarSiemens Shenzhen Magnetic Resonance , Ltd.K262622Swoop® Portable MR Imaging® SystemHyperfine, Inc.K254250MagicScan-1.5, GreenMR Serenity 1.5TXingaoyi Medical Equipment Co.,LtdK253808AIR Recon DLGE Medical Systems

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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