Last synced on 25 January 2026 at 3:41 am

CURITY PERCUTANEOUS CATHETER INSERTION KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K855061
510(k) Type
Traditional
Applicant
THE KENDAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1986
Days to Decision
119 days

CURITY PERCUTANEOUS CATHETER INSERTION KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K855061
510(k) Type
Traditional
Applicant
THE KENDAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1986
Days to Decision
119 days