FDA 510(k) Applications Submitted by MEDTRONIC CARDIAC SURGERY, MEDTRONIC, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960755 | 02/23/1996 | CARDIOTHERM BLOOD CARDIOPLEGIA SYSTEMS | MEDTRONIC CARDIAC SURGERY, MEDTRONIC, INC. |
| K953564 | 07/31/1995 | MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE | MEDTRONIC CARDIAC SURGERY, MEDTRONIC, INC. |
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