K172590 is an FDA 510(k) clearance for the Spectra Optia Apheresis System, a Separator, Automated, Blood Cell And Plasma, Therapeutic, submitted by Terumobct, Inc. (Lakewood, US). The FDA issued a Cleared decision on March 2, 2018, 185 days after receiving the submission on August 29, 2017. This device falls under the Gastroenterology & Urology review panel.
| 510(k) Number | K172590 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 29, 2017 |
| Decision Date | March 02, 2018 |
| Days to Decision | 185 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | LKN — Separator, Automated, Blood Cell And Plasma, Therapeutic |
| Device Class | — |