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INSPIRE 8 DUAL HOLLOW FIBER OXYGENATOR WITH WITH INTEGRATED HARDSHELL VENOUS/CARDIOTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121229
510(k) Type
Traditional
Applicant
SORIN GROUP ITALIA S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2012
Days to Decision
90 days
Submission Type
Summary

INSPIRE 8 DUAL HOLLOW FIBER OXYGENATOR WITH WITH INTEGRATED HARDSHELL VENOUS/CARDIOTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121229
510(k) Type
Traditional
Applicant
SORIN GROUP ITALIA S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2012
Days to Decision
90 days
Submission Type
Summary