CORDIS PTCA GUIDING CATHETER, MODIFICATION— 510(k) K913783

Substantially Equivalent

Dow Corning Wright

FDA 510(k) clearance K913783 for CORDIS PTCA GUIDING CATHETER, MODIFICATION, Substantially Equivalent on 1991-10-18. Applicant: Dow Corning Wright.

Clearance details

Applicant: Dow Corning Wright
Product code: Code DQY
Advisory panel: Cardiovascular
Date received: 1991-08-14
Decision date: 1991-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, US

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Adverse events under product code DQY

product code DQY

Death: 464
Injury: 4,489
Malfunction: 13,721
Other: 2
Total: 18,676

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.