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FDA 510(k)

MAGNETIC RESONANCE THERAPY DEVICE

K-Number: K903675 · 1991-01-17

ApplicantMrt, Inc.
Decision Date1991-01-17
Product CodeILX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESONANCE THERAPY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Mrt, Inc.. It received FDA 510(k) clearance on 1991-01-17 under 510(k) number K903675. The device is classified under product code ILX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNETIC RESONANCE THERAPY DEVICE?

MAGNETIC RESONANCE THERAPY DEVICE is a medical device that received FDA 510(k) clearance on 1991-01-17. The listed applicant is Mrt, Inc.. The 510(k) number is K903675.

When did MAGNETIC RESONANCE THERAPY DEVICE receive FDA 510(k) clearance?

MAGNETIC RESONANCE THERAPY DEVICE received FDA 510(k) clearance on 1991-01-17, under 510(k) number K903675.

Who is the listed applicant for MAGNETIC RESONANCE THERAPY DEVICE?

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

What is the FDA product code for MAGNETIC RESONANCE THERAPY DEVICE?

The FDA product code for MAGNETIC RESONANCE THERAPY DEVICE is ILX.

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Related Devices (Code: ILX)

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.

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Official Source

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

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