Phased Array/Bilateral Quadrature Contour Coil

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K932091 ↗

FDA Product Code

LNH

Device Class

Class II

Regulation

21 CFR Part 892.1000

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Quadrature Cervical Contour Coil

  Class II

  FDA 510(k) K923881 Active Cleared 5 Nov 1992

• Qquadrature Lumbar Contour Coil

  Class II

  FDA 510(k) K922006 Active Cleared 29 Jul 1992

• Anterior Neck Contour Coil

  Class II

  FDA 510(k) K905512 Active Cleared 7 Mar 1991

• Bilateral Temporal Mandibular Joint Coil

  Class II

  FDA 510(k) K930991 Active Cleared 18 Jun 1993

• Telerad Stat

  Class I

  FDA 510(k) K931795 Active Cleared 19 Nov 1993

• Quadrature Shoulder Contour Coil

  Class II

  FDA 510(k) K920227 Active Cleared 24 Aug 1992

See all devices from Magnetic Research, Inc. →

• What is the Phased Array/Bilateral Quadrature Contour Coil used for?

  This device is a contour coil designed specifically for phased array and bilateral quadrature configurations in Nuclear Magnetic Resonance Imaging (MRI) systems, intended for use in radiology settings.

• How is the Phased Array/Bilateral Quadrature Contour Coil supplied?

  The device is supplied by Magnetic Research, Inc. and is designed for integration with MRI systems to enhance imaging capabilities through its specialized contour coil technology.

• What is the regulatory status of this device?

  The Phased Array/Bilateral Quadrature Contour Coil received FDA 510(k) clearance with K932091 on December 14, 1993, and is classified as a Class II device under regulation 892.1000 for Systems for Nuclear Magnetic Resonance Imaging.

• Is this device reusable or single-use?

  The device data does not specify whether this contour coil is designed for single-use or multiple uses, as this information is not included in the provided specifications.