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NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953597
510(k) Type
Traditional
Applicant
MEADOX MEDICALS, DIV. BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1995
Days to Decision
67 days
Submission Type
Summary

NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953597
510(k) Type
Traditional
Applicant
MEADOX MEDICALS, DIV. BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1995
Days to Decision
67 days
Submission Type
Summary