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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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