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MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953564
510(k) Type
Traditional
Applicant
MEDTRONIC CARDIAC SURGERY, MEDTRONIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1996
Days to Decision
186 days
Submission Type
Summary

MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953564
510(k) Type
Traditional
Applicant
MEDTRONIC CARDIAC SURGERY, MEDTRONIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1996
Days to Decision
186 days
Submission Type
Summary