Last synced on 2 May 2025 at 11:05 pm

SURGITEK SUPER DOUBLE J URETERAL STENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880660
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1988
Days to Decision
57 days

SURGITEK SUPER DOUBLE J URETERAL STENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880660
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1988
Days to Decision
57 days