Last synced on 25 November 2022 at 11:04 pm

UROTECH CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911617
510(k) Type
Traditional
Applicant
UROTECH U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1993
Days to Decision
686 days

UROTECH CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911617
510(k) Type
Traditional
Applicant
UROTECH U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1993
Days to Decision
686 days