K971516

Substantially Equivalent

CORDIS POWERFLEX PLUS PTA BALLOON CATHETER

Applicant: Cordis Corp.
Product code: LIT
Advisory panel: Cardiovascular
Date received: 1997-04-28
Decision date: 1997-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami Lakes, FL, US

Adverse events under product code LIT

product code LIT

Death: 27
Injury: 1,256
Malfunction: 12,127
Total: 13,410

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.