Minntech Corp.
FDA 510(k) & PMA Approved Devices — 33 products
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Total Devices33
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120306 | RAPICIDE OPA-28 | MED | 2012-09-27 | View |
| 510(k) | K092387 | MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM | FEB | 2010-04-05 | View |
| 510(k) | K071298 | HF JUNIOR HEMOFILTER | KDI | 2007-08-08 | View |
| 510(k) | K050952 | HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR | KDI | 2006-01-31 | View |
| 510(k) | K033505 | RENACLEAN SH DIALYZER CLEANING SYSTEM | LIF | 2004-04-27 | View |
| 510(k) | K014016 | ENGUARD CHC DUAL RESERVOIR CARDIOPLEGIA HEATER/COOLER | DWC | 2002-02-01 | View |
| 510(k) | K991137 | ENGUARD PHX CARDIOPLEGIA HEAT EXCHANGER | DTR | 2000-06-08 | View |
| 510(k) | K000028 | RENAFLO II HF 2000 HEMOFILTER | KDI | 2000-04-04 | View |
| 510(k) | K991851 | RENACLEAR DIALYZER CLEANING SYSTEM | LIF | 1999-08-30 | View |
| 510(k) | K983126 | FIBERFLO HOLLOW FIBER CAPSULE WATER FILTERS | FIP | 1999-03-08 | View |
| 510(k) | K983085 | HEMOCOR HPH 700 HEMOCONCENTRATOR | KDI | 1998-11-13 | View |
| 510(k) | K980859 | HEMOCOR HPH MINI HEMOCONCENTRATOR | KDI | 1998-05-12 | View |
| 510(k) | K960513 | PERACT 20 LIQUID STERILANT | MED | 1997-10-01 | View |
| 510(k) | K972017 | BIOCOR SOFTSHELL VENOUS RESERVOIR (BIOCOR SVR) | DTN | 1997-09-10 | View |
| 510(k) | K964967 | BIOCOR 200 HIGH PERFORMANCEOXYGENATOR | DTZ | 1997-03-06 | View |
| 510(k) | K962707 | MINNTECH MINNIFILTER PLUS HEMOFILTER AND TUBING SET | KDI | 1996-10-09 | View |
| 510(k) | K953821 | BIOCOR 200 HARDSHELL VENOUS RESERVIOR | DTN | 1996-03-07 | View |
| 510(k) | K954349 | FIBERFLO HOLLOW FIBER CARTRIDGE WATER FILTERS | FIP | 1995-12-15 | View |
| 510(k) | K941439 | RENALIN COLD STERILANT | LRJ | 1995-06-26 | View |
| 510(k) | K945136 | RENAGUARD DIALYSATE FILTER | FIP | 1995-02-28 | View |
No matching devices.
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