meddevicedb.com FDA Device Reference

Reusable SPO2 Sensor (BSA307-47; BSA109-50; BSA109-31O)

K253109 Class II Traditional
Decision Date
2026-01-07
Sponsor / Applicant
Shenzhen Best Electronics Co., Ltd.

Technical Specification

510(k) Submission ID K253109
Product Code DQA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 2026-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Reusable SPO2 Sensor (BSA307-47; BSA109-50; BSA109-31O) received FDA 510(k) clearance under submission number K253109, sponsored by Shenzhen Best Electronics Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2026-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.