Pulse Oximeter(Model OHT60,OXH78)— 510(k) K230277

Substantially Equivalent

Cofoe Medical Technology Co., Ltd.

FDA 510(k) clearance K230277 for Pulse Oximeter(Model OHT60,OXH78), Substantially Equivalent on 2024-01-04. Applicant: Cofoe Medical Technology Co., Ltd..

Clearance details

Applicant: Cofoe Medical Technology Co., Ltd.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2023-02-01
Decision date: 2024-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Changsha, 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.