Electronic Blood Pressure Monitor (BP-204C, BP-204A, BP-215, BP-203C, BP-205A, BP-201C, BP-217, BP-202C, BP-202 BP-205, BP-205B,BP-206)— 510(k) K260470

Substantially Equivalent

Shenzhen Brav Electronic Technologies Co., Ltd.

FDA 510(k) clearance K260470 for Electronic Blood Pressure Monitor (BP-204C, BP-204A, BP-215, BP-203C, BP-205A, BP-201C, BP-217, BP-202C, BP-202 BP-205, BP-205B,BP-206), Substantially Equivalent on 2026-10-01. Applicant: Shenzhen Brav Electronic Technologies Co., Ltd.. Device class: 2.

Summary

Shenzhen Brav Electronic Technologies' Electronic Blood Pressure Monitor is cleared across a dozen model numbers, including BP-201C, BP-215, and BP-206. Product code DXN is non-invasive blood pressure measurement systems.

Class II, 21 CFR 870.1130. The Cardiovascular panel reviewed it as a Traditional 510(k).

The company filed from Shenzhen, China. Review took 231 days (February 12 to October 1, 2026).

Clearance details

Applicant
Shenzhen Brav Electronic Technologies Co., Ltd.
Product code
Product code DXN
Device class
Class 2
Regulation
21 CFR 870.1130
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shenzhen, CN
Download summary PDFView on FDA.gov ↗

Recent devices under product code DXN

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More clearances from Shenzhen Brav Electronic Technologies Co., Ltd.

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Adverse events under product code DXN

product code DXN
Death
3
Injury
169
Malfunction
1,019
Other
2
Total
1,193

Source: openFDA MAUDE database, through . 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.