FDA 510(k) Applications Submitted by RENAL SYSTEMS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970648 | 02/20/1997 | PRIMUS HOLLOW FIBER DIALYZER (MODELS 1000,1000S,1350,1350S,2000,2000S) | RENAL SYSTEMS, INC. |
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