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SILICONE BILIARY STENT/BILIARY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973114
510(k) Type
Traditional
Applicant
SPECIALTY SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1997
Days to Decision
30 days
Submission Type
Statement

SILICONE BILIARY STENT/BILIARY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973114
510(k) Type
Traditional
Applicant
SPECIALTY SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1997
Days to Decision
30 days
Submission Type
Statement