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STERILE SODIUM CHLORIDE 0.9% FLUSH, 5ML, 10ML, AMPULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082689
510(k) Type
Traditional
Applicant
Spectra Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2009
Days to Decision
186 days
Submission Type
Summary

STERILE SODIUM CHLORIDE 0.9% FLUSH, 5ML, 10ML, AMPULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082689
510(k) Type
Traditional
Applicant
Spectra Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2009
Days to Decision
186 days
Submission Type
Summary