MAGNETIC RESONANCE THERAPY DEVICE— 510(k) K903675

Substantially Equivalent

Mrt, Inc.

FDA 510(k) clearance K903675 for MAGNETIC RESONANCE THERAPY DEVICE, Substantially Equivalent on 1991-01-17. Applicant: Mrt, Inc.. Device class: 2.

Clearance details

Applicant: Mrt, Inc.
Product code: Code ILX
Device class: Class 2
Regulation: 21 CFR 890.5290
Advisory panel: Physical Medicine
Date received: 1990-08-13
Decision date: 1991-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Monica, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.