PLEXUS 2 & 3.5 HOLLOW FIBER OXYGENATORS— 510(k) K931444

Substantially Equivalent

Sorin Biomedica, Fiat, USA, Inc.

FDA 510(k) clearance K931444 for PLEXUS 2 & 3.5 HOLLOW FIBER OXYGENATORS, Substantially Equivalent on 1994-05-27. Applicant: Sorin Biomedica, Fiat, USA, Inc..

Clearance details

Applicant: Sorin Biomedica, Fiat, USA, Inc.
Product code: Code DTZ
Advisory panel: Cardiovascular
Date received: 1993-03-22
Decision date: 1994-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DTZ

product code DTZ

Death: 182
Injury: 422
Malfunction: 3,636
Total: 4,240

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.