MRX-750— 510(k) K933162

Name: FDA 510(k) clearance K933162
Creator: U.S. Food and Drug Administration
Published: 1993-10-07

Substantially Equivalent

Mrx Corp.

FDA 510(k) clearance K933162 for MRX-750, Substantially Equivalent on 1993-10-07. Applicant: Mrx Corp.. Device class: 1.

Clearance details

Applicant: Mrx Corp.
Product code: Code ITY
Device class: Class 1
Regulation: 21 CFR 892.1760
Advisory panel: Radiology
Date received: 1993-06-29
Decision date: 1993-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ITY

product code ITY

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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