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MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011283
510(k) Type
Traditional
Applicant
THE KENDALL COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2001
Days to Decision
171 days
Submission Type
Summary

MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011283
510(k) Type
Traditional
Applicant
THE KENDALL COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2001
Days to Decision
171 days
Submission Type
Summary