The following data is part of a premarket notification filed by Paragonix Technologies, Inc. with the FDA for Sherpa Pak Transporter.
| Device ID | K133694 |
| 510k Number | K133694 |
| Device Name: | SHERPA PAK TRANSPORTER |
| Classification | System, Perfusion, Kidney |
| Applicant | PARAGONIX TECHNOLOGIES, INC. 93 BENEFIT STREET Providence, RI 02904 |
| Contact | Leo Basta |
| Correspondent | Leo Basta PARAGONIX TECHNOLOGIES, INC. 93 BENEFIT STREET Providence, RI 02904 |
| Product Code | KDN |
| CFR Regulation Number | 876.5880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-12-03 |
| Decision Date | 2014-05-23 |
| Summary: | summary |