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SURECATH - ITP II PERCUTANEOUS PORT ACCESS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875213
510(k) Type
Traditional
Applicant
TITAN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1988
Days to Decision
76 days

SURECATH - ITP II PERCUTANEOUS PORT ACCESS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875213
510(k) Type
Traditional
Applicant
TITAN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1988
Days to Decision
76 days