Protocol Systems, Inc.
FDA 510(k) & PMA Approved Devices — 15 products
Advertisement
Total Devices15
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K002725 | MICROPAQ, MODELS 402 AND 404 | DRT | 2000-11-21 | View |
| 510(k) | K972121 | ACUITY CENTRAL STATION | MLD | 1997-11-07 | View |
| 510(k) | K951246 | PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS | FLS | 1996-02-02 | View |
| 510(k) | K945071 | PROPAQ 200 MONITOR | DRT | 1995-05-10 | View |
| 510(k) | K935846 | MODEL ACUITY CENTRAL STATION | DSI | 1994-12-05 | View |
| 510(k) | K934711 | PROPAQ ECG TELEMETRY OPTION | DRG | 1994-09-01 | View |
| 510(k) | K921497 | PROPAQ MONITORS, MODIFICATION | CCK | 1993-03-23 | View |
| 510(k) | K914838 | PROPAQ 102,104,106,102EL,104EL,&106EL | MHX | 1992-01-10 | View |
| 510(k) | K913193 | MODEL 100 CENTRAL STATION | DQK | 1991-10-16 | View |
| 510(k) | K910882 | PROPAQ 102EL, 104EL AND 106EL | DRT | 1991-05-08 | View |
| 510(k) | K910772 | PROPAQ 102, 104 AND 106 | DXN | 1991-04-12 | View |
| 510(k) | K902730 | SPO2 OPTION | DQA | 1990-10-22 | View |
| 510(k) | K894607 | PAQ10 PAPER CHART RECORDER | DSF | 1989-10-26 | View |
| 510(k) | K884320 | PROPAQ 106(TM) | DRT | 1988-12-27 | View |
| 510(k) | K882085 | PROPAQ 104(TM) | DSK | 1988-07-28 | View |
No matching devices.
Advertisement