MASIMO ROOT MONITORING SYSTEM— 510(k) K140188

Name: FDA 510(k) clearance K140188
Creator: U.S. Food and Drug Administration
Published: 2014-06-25

Substantially Equivalent

Masimo Corporation

FDA 510(k) clearance K140188 for MASIMO ROOT MONITORING SYSTEM, Substantially Equivalent on 2014-06-25. Applicant: Masimo Corporation. Device class: 2.

Clearance details

Applicant: Masimo Corporation
Product code: Code MWI
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 2014-01-24
Decision date: 2014-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MWI

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K260438 — Vital Signs Monitor (CLEO2)2026-08-14
K253417 — Masimo Root Monitoring System2026-08-12
K253196 — Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)2026-06-12
K253436 — c-med0 alpha2026-04-30
K250135 — WAVE Clinical Platform (2.0.000)2026-01-16

More clearances from Masimo Corporation

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K260880 — SedLine Sedation Monitor2026-07-10
K254209 — Radius VSM and Accessories2026-06-04
K243324 — Masimo O3 Regional Oximeter2025-07-17
K250757 — Radius VSM and Accessories2025-05-29
K243305 — Masimo W12025-04-03

Adverse events under product code MWI

product code MWI

Death: 16
Malfunction: 963
Total: 979

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.