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Cleveland Multiport Ventricular Catheter Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161731
510(k) Type
Traditional
Applicant
Parker Hannifin Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2017
Days to Decision
277 days
Submission Type
Summary

Cleveland Multiport Ventricular Catheter Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161731
510(k) Type
Traditional
Applicant
Parker Hannifin Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2017
Days to Decision
277 days
Submission Type
Summary