BD PREEFILE NORMAL SALINE FLUSH SYRINGE FLUSH SYRINGE— 510(k) K982558

Substantially Equivalent

Bd/Preefil

FDA 510(k) clearance K982558 for BD PREEFILE NORMAL SALINE FLUSH SYRINGE FLUSH SYRINGE, Substantially Equivalent on 2000-03-08. Applicant: Bd/Preefil.

Clearance details

Applicant: Bd/Preefil
Product code: Code FOZ
Advisory panel: General Hospital
Date received: 1998-07-22
Decision date: 2000-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, 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.