K920889

Substantially Equivalent

MINIMAX(R)/MAXIMA(R) HOLLOW FIBER OXYGENATORS

Applicant: Medtronic Vascular
Product code: DTZ
Advisory panel: Cardiovascular
Date received: 1992-02-12
Decision date: 1992-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

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.