FDA 510(k) Applications Submitted by THORATEC CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K152161 | 08/03/2015 | Thoratec CentriMag Return (Arterial) Cannula Kit | Thoratec Corporation |
| K152190 | 08/05/2015 | Thoratec CentriMag Drainage (Venous) Cannula Kit | THORATEC CORPORATION |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact