HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M— 510(k) K100203

Substantially Equivalent

Beijing Choice Electronic Technololgy Co., Ltd.

FDA 510(k) clearance K100203 for HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M, Substantially Equivalent on 2010-05-17. Applicant: Beijing Choice Electronic Technololgy Co., Ltd..

Clearance details

Applicant: Beijing Choice Electronic Technololgy Co., Ltd.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2010-01-25
Decision date: 2010-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shanghai, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.