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0.9% SODIUM CHLORIDE INJECTION, USP BD POSIFLUSH; SP SYRINGE, SF SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141311
510(k) Type
Special
Applicant
Becton, Dickinson and Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2014
Days to Decision
66 days
Submission Type
Summary

0.9% SODIUM CHLORIDE INJECTION, USP BD POSIFLUSH; SP SYRINGE, SF SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141311
510(k) Type
Special
Applicant
Becton, Dickinson and Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2014
Days to Decision
66 days
Submission Type
Summary