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KENSEY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880194
510(k) Type
Traditional
Applicant
THERATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1988
Days to Decision
90 days

KENSEY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880194
510(k) Type
Traditional
Applicant
THERATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1988
Days to Decision
90 days