Mennen Medical, Inc.
FDA 510(k) & PMA Approved Devices — 34 products
Advertisement
Total Devices34
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K030722 | ENVOY PATIENT MONITOR | MHX | 2004-02-26 | View |
| 510(k) | K983864 | ETCO2 VITAL SIGNS MODULE | CCK | 1999-10-08 | View |
| 510(k) | K991775 | MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS | DXG | 1999-06-24 | View |
| 510(k) | K982697 | MODIFICATION TO ENSEMBLE CENTRAL STATION MONITOR | DSI | 1998-08-12 | View |
| 510(k) | K974510 | ENVOY PATIENT MONITOR | DSI | 1998-04-14 | View |
| 510(k) | K970358 | ENSEMBLE CENTRAL STATION MONITOR | DSI | 1998-02-11 | View |
| 510(k) | K940081 | MERCURY | DRT | 1995-04-12 | View |
| 510(k) | K940415 | HORIZON 9000 WS | DXG | 1995-01-06 | View |
| 510(k) | K920915 | CAPNOMED 100 STAND-ALONE ETCO2 MODULE | CCK | 1993-03-23 | View |
| 510(k) | K914381 | HORIZON 9000/HIS OPTION AMPLIFIER | DRR | 1992-01-28 | View |
| 510(k) | K913339 | HORIZON PACEMAKER DETECTION SOFTWARE | DSI | 1992-01-08 | View |
| 510(k) | K911257 | MR-5200 FULL DISCLOSURE SYSTEM | DSH | 1991-08-19 | View |
| 510(k) | K910945 | HORIZON 2000 EEG MONITORING OPTION | GWQ | 1991-08-15 | View |
| 510(k) | K911616 | HORIZON XL | DRT | 1991-07-10 | View |
| 510(k) | K903524 | HORIZON 2000 ST ANALYSIS OPTION | DPS | 1991-03-01 | View |
| 510(k) | K901774 | HORIZON 2000 PULSE OXIMETRY (SAO2) MONITOR CAPABIL | DQA | 1990-05-22 | View |
| 510(k) | K895895 | MODEL 219 TELEMETRY SYSTEM | GYE | 1990-02-22 | View |
| 510(k) | K894918 | HORIZON 2000 FRACTION OF INSPIRED OXYGEN MON. CAP. | CCL | 1989-10-31 | View |
| 510(k) | K893585 | 14 COLOR VIDEO DISPLAY 211-260-010 | LLZ | 1989-07-20 | View |
| 510(k) | K893133 | HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX | KLK | 1989-07-14 | View |
No matching devices.
Advertisement