K080206

Substantially Equivalent

MODIFICATION TO FEMOSTOP FEMORAL COMPRESSION SYSTEM

Applicant: Radi Medical Systems AB
Product code: DXC
Advisory panel: Cardiovascular
Date received: 2008-01-28
Decision date: 2008-02-26
Decision: Substantially Equivalent
Clearance type: Special
Location: Uppsala, SE

Adverse events under product code DXC

product code DXC

Death: 14
Injury: 442
Malfunction: 2,209
Other: 1
Total: 2,666

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.