meddevicedb.com FDA Device Reference

Blood Pressure Monitor (BBZ32-AA01)

K240832 Class II Traditional
Decision Date
2024-06-07
Sponsor / Applicant
Guangdong Transtek Medical Electronics Co., Ltd.

Technical Specification

510(k) Submission ID K240832
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2024-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Blood Pressure Monitor (BBZ32-AA01) received FDA 510(k) clearance under submission number K240832, sponsored by Guangdong Transtek Medical 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 2024-06-07.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.