Pace Tech, Inc.
FDA 510(k) & PMA Approved Devices — 18 products
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Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K951226 | VITALMAX 4000/MINIPACK 3100/3000 | DSK | 1996-11-21 | View |
| 510(k) | K953795 | VITALMAX 4100 | CBS | 1996-07-01 | View |
| 510(k) | K944541 | HANDYPACK 911SC | CCK | 1995-02-22 | View |
| 510(k) | K945385 | VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300 | MHX | 1995-01-31 | View |
| 510(k) | K925701 | MINIPACK 911-STC | CCK | 1994-08-11 | View |
| 510(k) | K934385 | MINIPACK 3100/3000 MODIFICATION | DXN | 1994-08-10 | View |
| 510(k) | K933624 | VITALMAX 4000 | MHX | 1994-07-19 | View |
| 510(k) | K930559 | VITALMAX 800-C | CCK | 1993-09-03 | View |
| 510(k) | K912835 | MINI-PACK 911 SERIES | MHX | 1992-02-03 | View |
| 510(k) | K912880 | VITALMAX 510/520 | DQA | 1991-11-14 | View |
| 510(k) | K913263 | VITALMAX 830 SERIES | MHX | 1991-10-10 | View |
| 510(k) | K905274 | VITALMAX 2100/2200 | DRT | 1991-07-17 | View |
| 510(k) | K901066 | VITALMAX 500 PULSE OXIMETER W/TEMP. AND RESPIRA. | DQA | 1990-08-28 | View |
| 510(k) | K900451 | VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE | DRT | 1990-07-18 | View |
| 510(k) | K901612 | VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE | DQA | 1990-04-30 | View |
| 510(k) | K900866 | OXIMAX 700 | DQA | 1990-04-04 | View |
| 510(k) | K900843 | OXIMAX 100 | DQA | 1990-03-28 | View |
| 510(k) | K880351 | VITAL SYSTEM | DXN | 1988-03-22 | View |
No matching devices.
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