FDA 510(k) Applications Submitted by JAN L ZORN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010131 | 01/16/2001 | PHD PERSONAL HEMODIALYSIS INSTRUMENT-1M101, PHD WATER PRE-TREATMENT KIT-1W605,PHD HARD PLUMBING KIT-1W604, PHD BLOOD TUB | AKSYS, LTD. |
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