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OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851647
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1985
Days to Decision
72 days

OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K851647
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1985
Days to Decision
72 days