Last synced on 25 November 2022 at 11:04 pm

URETERAL BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903813
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1990
Days to Decision
79 days

URETERAL BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903813
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1990
Days to Decision
79 days