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NON-PVC FLUID PATH PORT ACCESS INFUSION SET WITH SLIT SEPTUM INJECTION SITE

Page Type
Cleared 510(K)
510(k) Number
K964117
510(k) Type
Traditional
Applicant
KAWASUMI LABORATORIES CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1997
Days to Decision
150 days
Submission Type
Summary

NON-PVC FLUID PATH PORT ACCESS INFUSION SET WITH SLIT SEPTUM INJECTION SITE

Page Type
Cleared 510(K)
510(k) Number
K964117
510(k) Type
Traditional
Applicant
KAWASUMI LABORATORIES CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1997
Days to Decision
150 days
Submission Type
Summary