Last synced on 14 November 2025 at 11:06 pm

UROTECH CATHETER

Page Type
Cleared 510(K)
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)
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