NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUS— 510(k) K130879

Substantially Equivalent

Nexus Medical, LLC

FDA 510(k) clearance K130879 for NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUS, Substantially Equivalent on 2013-07-09. Applicant: Nexus Medical, LLC.

Clearance details

Applicant: Nexus Medical, LLC
Product code: Code FPA
Advisory panel: General Hospital
Date received: 2013-03-29
Decision date: 2013-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

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Adverse events under product code FPA

product code FPA

Death: 95
Injury: 14,421
Malfunction: 125,815
Other: 30
Total: 140,361

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.