510(k) Report

FDA applicant

Beijing Choice Electronic Technology Co., Ltd.

Beijing, CN14 decisions2016–20240 recalls

FDA records 14 decisions for Beijing Choice Electronic Technology Co., Ltd. (Beijing, CN) from 2016 to 2024: 14 510(k) clearances. Most are in product codes DQA (Oximeter) and DXN (System, Measurement, Blood-Pressure…). Since 2016 its 510(k)s took a median of 223 days from receipt to decision, against 253 for FDA’s reviews in the same codes and years. Its devices cite 15 predicates, 5 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 Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2016: 32017: 12018: 22021: 12022: 32023: 32024: 1
2016high 3 (2016) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Beijing Choice Electronic Technology Co., Ltd. by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report