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UROSURGE SPIRASTENT PLUS URETERAL STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981489
510(k) Type
Traditional
Applicant
UROSURGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1998
Days to Decision
32 days
Submission Type
Statement

UROSURGE SPIRASTENT PLUS URETERAL STENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981489
510(k) Type
Traditional
Applicant
UROSURGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1998
Days to Decision
32 days
Submission Type
Statement