NEUTRAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH NEUTRAL LUER ACTIVATED DEVICE— 510(k) K120443

Substantially Equivalent

Baxter Healthcare Corporation - Renal Division

FDA 510(k) clearance K120443 for NEUTRAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH NEUTRAL LUER ACTIVATED DEVICE, Substantially Equivalent on 2012-05-22. Applicant: Baxter Healthcare Corporation - Renal Division.

Clearance details

Applicant: Baxter Healthcare Corporation - Renal Division
Product code: Code FPA
Advisory panel: General Hospital
Date received: 2012-02-14
Decision date: 2012-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mcgaw Park, IL, 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.