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OLBERT CATHETER SYS FOR URETERAL DILATION

Page Type
Cleared 510(K)
510(k) Number
K851463
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1985
Days to Decision
38 days

OLBERT CATHETER SYS FOR URETERAL DILATION

Page Type
Cleared 510(K)
510(k) Number
K851463
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1985
Days to Decision
38 days