Cobe Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 77 products
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Total Devices77
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K923272 | COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATOR | DTZ | 1993-05-11 | View |
| 510(k) | K900105 | COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTIC | LKN | 1991-03-22 | View |
| 510(k) | K905793 | COBE CENTRY 2 BICART OPTION KIT | FKP | 1991-02-12 | View |
| 510(k) | K905388 | COBE CENTRYSYSTEM 3 BICART OPTION KIT | FKP | 1991-02-11 | View |
| 510(k) | K904336 | NEW COBE SATURATION/HEMATOCRIT MONITOR | GKF | 1990-12-27 | View |
| 510(k) | K902631 | COBE ICU CONVERSION KIT | DTN | 1990-12-17 | View |
| 510(k) | K902437 | COBE CARDIOTOMY RESERVOIR WITH OR WITHOUT FILTER | DTP | 1990-12-17 | View |
| 510(k) | K904566 | NEW COBE CENTRYSYSTEM(TM) 100 HG DIALYZER | FJI | 1990-12-12 | View |
| 510(k) | K902758 | COBE SATURATION/HEMATOCRIT MONITOR W/ FIBER OPTIC | DQA | 1990-08-23 | View |
| 510(k) | K902759 | COBE CLOSED WOUND DRAINAGE KIT | CAC | 1990-07-18 | View |
| 510(k) | K902671 | COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER | CAC | 1990-07-17 | View |
| 510(k) | K900910 | COBE AIR EMBOLI PROTECTION SYSTEM (AEPS) | DTW | 1990-05-22 | View |
| 510(k) | K900758 | HEPARINIZED ARTERIAL SCREEN BLOOD FILTER | DTM | 1990-05-17 | View |
| 510(k) | K895076 | CMS VRB-1200 | DTN | 1989-11-03 | View |
| 510(k) | K893962 | COBE 2991 SUPPLEMENTARY DISPOSABLE SETS | LKN | 1989-10-18 | View |
| 510(k) | K881811 | COBE CENTRYSYSTEM HOLLOW FIBER DIALYZERS | FJI | 1988-09-15 | View |
| 510(k) | K881330 | COBE HEART/LUNG PERFUSION AND CARDIOPLEGIA PACK | DWF | 1988-06-10 | View |
| 510(k) | K881062 | CENTRY 2 ULTRAFILTRATION CONTROL KIT, #018762-002 | FJB | 1988-04-21 | View |
| 510(k) | K880021 | COBE CML3 | DTZ | 1988-04-01 | View |
| 510(k) | K870976 | ONGUARD 1000, CATALOG #043611-000 & 043611-001 | DTQ | 1987-05-06 | View |
No matching devices.
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