DUO-CATH FEMORAL— 510(k) K771573

Substantially Equivalent

Medical Device Laboratories

FDA 510(k) clearance K771573 for DUO-CATH FEMORAL, Substantially Equivalent on 1977-09-15. Applicant: Medical Device Laboratories.

Clearance details

Applicant: Medical Device Laboratories
Product code: Code FOZ
Advisory panel: General Hospital
Date received: 1977-08-15
Decision date: 1977-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.