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NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952884
510(k) Type
Traditional
Applicant
Meadox Medicals, Div. Boston Scientific Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1996
Days to Decision
243 days
Submission Type
Summary

NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952884
510(k) Type
Traditional
Applicant
Meadox Medicals, Div. Boston Scientific Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1996
Days to Decision
243 days
Submission Type
Summary