RETROGRADE CARDIOPLEGIA CANNULA, MANUAL-INFLATING, WITH MALLEABLE OR GUIDWIRE STYLET— 510(k) K010974

Substantially Equivalent

Sorin Group Italia S.R.L.

FDA 510(k) clearance K010974 for RETROGRADE CARDIOPLEGIA CANNULA, MANUAL-INFLATING, WITH MALLEABLE OR GUIDWIRE STYLET, Substantially Equivalent on 2001-06-18. Applicant: Sorin Group Italia S.R.L..

Clearance details

Applicant: Sorin Group Italia S.R.L.
Product code: Code DWF
Advisory panel: Cardiovascular
Date received: 2001-04-02
Decision date: 2001-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mirandola, IT

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Adverse events under product code DWF

product code DWF

Death: 106
Injury: 386
Malfunction: 2,323
Total: 2,815

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.