Digital Automatic Blood Pressure Monitor BPM30 and BPM31 Series— 510(k) K152483

Substantially Equivalent

Grandway Technology (Shenzhen) Limited

FDA 510(k) clearance K152483 for Digital Automatic Blood Pressure Monitor BPM30 and BPM31 Series, Substantially Equivalent on 2015-09-29. Applicant: Grandway Technology (Shenzhen) Limited. Device class: 2.

Clearance details

Applicant
Grandway Technology (Shenzhen) Limited
Product code
Code DXN
Device class
Class 2
Regulation
21 CFR 870.1130
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Shenzhen, CN
Download summary PDFView on FDA.gov ↗

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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.