K133694 is an FDA 510(k) clearance for the SHERPA PAK TRANSPORTER, a System, Perfusion, Kidney (Class II — Special Controls, product code KDN), submitted by Paragonix Technologies, Inc. (Providence, US). The FDA issued a Cleared decision on May 23, 2014, 171 days after receiving the submission on December 3, 2013. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5880.
| 510(k) Number | K133694 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | December 03, 2013 |
| Decision Date | May 23, 2014 |
| Days to Decision | 171 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | KDN — System, Perfusion, Kidney |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5880 |