Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Beijing Choice Electronic Technology Co., Ltd. — Predicate Candidate Screening
14 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
224 daysmedian FDA review time
282 days90th percentile
14clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K232975 | Pulse Oximeter (MD300C228) | Beijing Choice Electronic Technology Co., Ltd. | 2024-06-21 | 274 | 0 |
| K230587 | Wrist Pulse Oximeter | Beijing Choice Electronic Technology Co., Ltd. | 2023-11-30 | 273 | 0 |
| K230172 | Pulse Oximeter | Beijing Choice Electronic Technology Co., Ltd. | 2023-08-12 | 204 | 0 |
| K220101 | Pulse Oximeter | Beijing Choice Electronic Technology Co., Ltd. | 2023-03-08 | 420 | 0 |
| K221992 | Electronic Pulse Stimulator | Beijing Choice Electronic Technology Co., Ltd. | 2022-10-21 | 107 | 0 |
| K211400 | Pulse Oximeter | Beijing Choice Electronic Technology Co., Ltd. | 2022-02-11 | 282 | 0 |
| K211752 | Infrared Thermometer | Beijing Choice Electronic Technology Co., Ltd. | 2022-01-21 | 228 | 0 |
| K211754 | Vital Signs Monitor | Beijing Choice Electronic Technology Co., Ltd. | 2021-11-15 | 161 | 0 |
| K181503 | Fingertip Pulse Oximeter | Beijing Choice Electronic Technology Co., Ltd. | 2018-10-11 | 126 | 0 |
| K172366 | Wrist Pulse Oximeter | Beijing Choice Electronic Technology Co., Ltd. | 2018-03-16 | 224 | 0 |
| K162089 | Blood Pressure Monitor | Beijing Choice Electronic Technology Co., Ltd. | 2017-02-10 | 197 | 0 |
| K160268 | Fingertip Pulse Oximeter MD300CG11/MD300CG51 | Beijing Choice Electronic Technology Co., Ltd. | 2016-10-14 | 255 | 0 |
| K161560 | Fingertip Pulse Oximeter MD300CN310 | Beijing Choice Electronic Technology Co., Ltd. | 2016-10-05 | 121 | 0 |
| K152563 | Pulse Oximeter (MD300M/MD300K2) | Beijing Choice Electronic Technology Co., Ltd. | 2016-04-18 | 222 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda