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REDIFURL AND TEPERSEAL DL INTRA-AORTIC BALLOON CATHETERS WITH HYDROMER COATING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935184
510(k) Type
Traditional
Applicant
ST. JUDE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1995
Days to Decision
472 days
Submission Type
Statement

REDIFURL AND TEPERSEAL DL INTRA-AORTIC BALLOON CATHETERS WITH HYDROMER COATING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935184
510(k) Type
Traditional
Applicant
ST. JUDE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1995
Days to Decision
472 days
Submission Type
Statement