The following data is part of a premarket notification filed by Terumo America, Inc. with the FDA for Clirans Th13 Hollow Fiber Dialyzer.
| Device ID | K802122 |
| 510k Number | K802122 |
| Device Name: | CLIRANS TH13 HOLLOW FIBER DIALYZER |
| Classification | Dialyzer, Capillary, Hollow Fiber |
| Applicant | TERUMO AMERICA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FJI |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-04 |
| Decision Date | 1980-12-18 |