Last synced on 25 January 2026 at 3:41 am

SODIUM CHLORIDE INJECTION, 0.9%, USP 5 ML, 10 ML AMPULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103740
510(k) Type
Traditional
Applicant
Spectra Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2011
Days to Decision
219 days
Submission Type
Summary

SODIUM CHLORIDE INJECTION, 0.9%, USP 5 ML, 10 ML AMPULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103740
510(k) Type
Traditional
Applicant
Spectra Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2011
Days to Decision
219 days
Submission Type
Summary