FDA.reportPublic FDA data

Device Listing 1012709256

Listing Summary#

Listing key
1012709256
Premarket submission
K250884
Device
0.9 % Sodium Chloride Injection, USP, BD PosiFlush™ SP Syringe
Applicant
Becton, Dickinson and Company
Product code
NGT
Decision date
2025-12-02