VITAL SIGNS MONITOR— 510(k) K113833

Name: FDA 510(k) clearance K113833
Creator: U.S. Food and Drug Administration
Published: 2012-05-01

Substantially Equivalent

Guangdong Biolight Meditech Co., Ltd.

FDA 510(k) clearance K113833 for VITAL SIGNS MONITOR, Substantially Equivalent on 2012-05-01. Applicant: Guangdong Biolight Meditech Co., Ltd.. Device class: 2.

Clearance details

Applicant: Guangdong Biolight Meditech Co., Ltd.
Product code: Code MWI
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 2011-12-27
Decision date: 2012-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shanghai, CN

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 Guangdong Biolight Meditech Co., Ltd.

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K181919 — Patient Monitor2019-04-05
K170514 — Central Monitoring System2017-05-24
K162234 — Truscope Ultra Patient Monitor2017-01-04
K160349 — Electronic Sphygmomanometer2016-11-03
K153580 — Central Monitoring System2016-09-07

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.