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MODIFIED LABELING OF CARDIAC ASSIST INTRA-AORTIC BALLOON CATHETERS: MODEL 930 - 940, 30 - 40 CC SENSATION AND NICATH 30C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963187
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1996
Days to Decision
82 days
Submission Type
Summary

MODIFIED LABELING OF CARDIAC ASSIST INTRA-AORTIC BALLOON CATHETERS: MODEL 930 - 940, 30 - 40 CC SENSATION AND NICATH 30C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963187
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1996
Days to Decision
82 days
Submission Type
Summary