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9.5 FR SIDEWINDER DL INTRA-AORTIC BALLON CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926000
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1993
Days to Decision
276 days
Submission Type
Summary

9.5 FR SIDEWINDER DL INTRA-AORTIC BALLON CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926000
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1993
Days to Decision
276 days
Submission Type
Summary