ROSSMAX MEDIPRO, MODELS 100F, 200F, AND 300F BLOOD PRESSURE MONITORS— 510(k) K013539

Substantially Equivalent

Rossmax International , Ltd.

FDA 510(k) clearance K013539 for ROSSMAX MEDIPRO, MODELS 100F, 200F, AND 300F BLOOD PRESSURE MONITORS, Substantially Equivalent on 2002-01-17. Applicant: Rossmax International , Ltd..

Clearance details

Applicant: Rossmax International , Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2001-10-24
Decision date: 2002-01-17
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Taipei, TW

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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, 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.