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MINIMAX(R)/MAXIMA(R) HOLLOW FIBER OXYGENATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920889
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1992
Days to Decision
216 days
Submission Type
Summary

MINIMAX(R)/MAXIMA(R) HOLLOW FIBER OXYGENATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920889
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1992
Days to Decision
216 days
Submission Type
Summary