Submission Details
| 510(k) Number | K130493 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 26, 2013 |
| Decision Date | March 13, 2013 |
| Days to Decision | 15 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
K130493 is an FDA 510(k) clearance for the CAPIOX RX05 HOLLOW FIBER OXYGENATOR/RESERVOIR, a Oxygenator, Cardiopulmonary Bypass (Class II — Special Controls, product code DTZ), submitted by Terumo Corporation (Elkton, US). The FDA issued a Cleared decision on March 13, 2013, 15 days after receiving the submission on February 26, 2013. This device falls under the Cardiovascular review panel. Regulated under 21 CFR 870.4350.
| 510(k) Number | K130493 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 26, 2013 |
| Decision Date | March 13, 2013 |
| Days to Decision | 15 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DTZ — Oxygenator, Cardiopulmonary Bypass |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 870.4350 |