Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Beijing Choice Electronic Technology with 43 510(k) clearances. The most recent is a 510(k) clearance dated Jun 21, 2024: Pulse Oximeter (MD300C228).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 21, 2024 | Pulse Oximeter (MD300C228)K232975 · DQA | 510(k) clearances |
| Nov 30, 2023 | Wrist Pulse OximeterK230587 · DQA | 510(k) clearances |
| Aug 12, 2023 | Pulse OximeterK230172 · DQA | 510(k) clearances |
| Mar 8, 2023 | Pulse OximeterK220101 · DQA | 510(k) clearances |
| Oct 21, 2022 | Electronic Pulse StimulatorK221992 · NUH | 510(k) clearances |
| Feb 11, 2022 | Pulse OximeterK211400 · DQA | 510(k) clearances |
| Jan 21, 2022 | Infrared ThermometerK211752 · FLL | 510(k) clearances |
| Nov 15, 2021 | Vital Signs MonitorK211754 · MWI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
