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0.9% Sodium Chloride Injection, USP BD PosiFlush™ SF Saline Flush Syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231161
510(k) Type
Traditional
Applicant
Becton, Dickinson and Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2023
Days to Decision
88 days
Submission Type
Summary

0.9% Sodium Chloride Injection, USP BD PosiFlush™ SF Saline Flush Syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231161
510(k) Type
Traditional
Applicant
Becton, Dickinson and Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2023
Days to Decision
88 days
Submission Type
Summary