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INDEFLATOR PLUS 30/PLUS 30 PRIORITY PACK9WITH THE.096 OR.115 ROTATING HEMOSTATIC VALVE)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962495
510(k) Type
Traditional
Applicant
Advanced Cardiovascular Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1996
Days to Decision
78 days
Submission Type
Summary

INDEFLATOR PLUS 30/PLUS 30 PRIORITY PACK9WITH THE.096 OR.115 ROTATING HEMOSTATIC VALVE)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962495
510(k) Type
Traditional
Applicant
Advanced Cardiovascular Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1996
Days to Decision
78 days
Submission Type
Summary