510(k) Report

FDA applicant

Beijing Choice Electronic Technololgy Co., Ltd.

Shanghai, CN29 decisions2007–20160 recalls

FDA records 29 decisions for Beijing Choice Electronic Technololgy Co., Ltd. (Shanghai, CN) from 2007 to 2016: 29 510(k) clearances. Most are in product codes DQA (Oximeter) and DPS (Electrocardiograph). Its devices cite 27 predicates, 15 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Beijing Choice Electronic Technololgy Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2007: 12008: 32009: 52010: 72011: 12012: 22013: 42014: 22015: 32016: 1
2007high 7 (2010) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Beijing Choice Electronic Technololgy Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Beijing Choice Electronic Technololgy…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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