Seratronics, Inc.
FDA 510(k) & PMA Approved Devices — 21 products
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Total Devices21
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K955299 | DPS 4 DIALYZER PREPARATION SYSTEM | LIF | 1996-10-21 | View |
| 510(k) | K931336 | DRS 4 DIALYZER REPROCESSING SYSTEM | LIF | 1996-04-18 | View |
| 510(k) | K944539 | DRS 4 ND DIALYZER REPROCESSING SYSTEM | LIF | 1995-11-29 | View |
| 510(k) | K923529 | DMS DATA MANAGEMENT SYSTEM/DRS-4 DIALYZER REPROCES | LIF | 1994-08-29 | View |
| 510(k) | K914580 | DRS-4 DIALYZER REPROCESSING SYSTEM | LIF | 1992-02-24 | View |
| 510(k) | K874573 | FRESENIUS PURISTERIL 340 (TM) | LIF | 1988-04-25 | View |
| 510(k) | K874872 | FRESENIUS HEMOFLOW F3, F4, F5, F7 | FJI | 1988-02-19 | View |
| 510(k) | K870725 | FRESENIUS HEMOFLOW F6 AND F8 | FJI | 1987-05-01 | View |
| 510(k) | K870724 | FRESENIUS HEMOFLOW F60 AND F80 | KDI | 1987-04-01 | View |
| 510(k) | K864587 | FRESENIUS ULTRAFLUX AV400, AV600 | KDI | 1987-03-03 | View |
| 510(k) | K864169 | FRESENIUS HEMOFLOW F50 & F70 | KDI | 1986-11-06 | View |
| 510(k) | K860674 | DRS-4 DIALYZER REPROCESSING SYSTEM | LIF | 1986-04-07 | View |
| 510(k) | K861106 | FRESENIUS HEMOFLOW F80 DIALYZER | KDI | 1986-04-07 | View |
| 510(k) | K855001 | FRESENIUS HEMODIALYSIS MACHINE A1008 BSM | FLC | 1986-01-21 | View |
| 510(k) | K853851 | FRESENIUS DISPOSABLE BLOOD LINES | FJK | 1985-11-12 | View |
| 510(k) | K852251 | FRESENIUS HEMOFLOW F60 & FRESENIUS HEMOFLOW F40 | KDI | 1985-07-25 | View |
| 510(k) | K844750 | FRESENIUS A2008 HEMODIALYSIS MACHINE EXPANSION MOD | FKQ | 1985-02-15 | View |
| 510(k) | K844641 | FRESENIUS HAEMODIALYSIS ;MACHINE A1008 | FKQ | 1985-02-14 | View |
| 510(k) | K843014 | FRESENIUS HAEMODIALYSIS A2008 | KDI | 1984-10-18 | View |
| 510(k) | K832230 | DIALYZER PREPARATION SYS DPS-4 | LIF | 1983-10-14 | View |
No matching devices.
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