Submission Details
| 510(k) Number | K220635 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 04, 2022 |
| Decision Date | November 16, 2022 |
| Days to Decision | 257 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
K220635 is an FDA 510(k) clearance for the Heater-Cooler System 3T, a Controller, Temperature, Cardiopulmonary Bypass (Class II — Special Controls, product code DWC), submitted by Livanova Deutschland, GmbH (Munchen, DE). The FDA issued a Cleared decision on November 16, 2022, 257 days after receiving the submission on March 4, 2022. This device falls under the Cardiovascular review panel. Regulated under 21 CFR 870.4250.
| 510(k) Number | K220635 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 04, 2022 |
| Decision Date | November 16, 2022 |
| Days to Decision | 257 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DWC — Controller, Temperature, Cardiopulmonary Bypass |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 870.4250 |
| Definition | If The Device Is Reusable, Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf). |