Vital Signs Monitor— 510(k) K211754

Name: FDA 510(k) clearance K211754
Creator: U.S. Food and Drug Administration
Published: 2021-11-15

Substantially Equivalent

Beijing Choice Electronic Technology Co., Ltd.

FDA 510(k) clearance K211754 for Vital Signs Monitor, Substantially Equivalent on 2021-11-15. Applicant: Beijing Choice Electronic Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Beijing Choice Electronic Technology Co., Ltd.
Product code: Code MWI
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 2021-06-07
Decision date: 2021-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, 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 Beijing Choice Electronic Technology Co., Ltd.

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K232975 — Pulse Oximeter (MD300C228)2024-06-21
K230587 — Wrist Pulse Oximeter2023-11-30
K230172 — Pulse Oximeter2023-08-12
K220101 — Pulse Oximeter2023-03-08
K221992 — Electronic Pulse Stimulator2022-10-21

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.