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SURGITEK(R) 4.5FR LUBRI-FLEX(TM) URETERAL STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913928
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1991
Days to Decision
77 days
Submission Type
Summary

SURGITEK(R) 4.5FR LUBRI-FLEX(TM) URETERAL STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913928
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1991
Days to Decision
77 days
Submission Type
Summary