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SILITEK URINARY DIVERSION STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840059
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1984
Days to Decision
26 days

SILITEK URINARY DIVERSION STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840059
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1984
Days to Decision
26 days