Epic Medical Equipment Services, Inc.
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K012333 | FLEXI-SITE SP02 EAR SENSOR | DPZ | 2001-10-17 | View |
| 510(k) | K002848 | SPO2 WRAP SENSOR | DQA | 2001-05-24 | View |
| 510(k) | K010718 | FLEXI-SITE SP02 EAR SENSOR | DPZ | 2001-03-23 | View |
| 510(k) | K002223 | EPIC SPO2 FINGER SENSOR, MODEL E412-20 | DQA | 2000-08-22 | View |
| 510(k) | K000831 | STAT-SHELL DISPOSABLE SP02 SENSOR | DQA | 2000-06-05 | View |
| 510(k) | K992811 | TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORING | HFM | 2000-01-18 | View |
| 510(k) | K992092 | STAT-SHELL DISPOSABLE SPO2 SENSOR | DQA | 1999-12-22 | View |
| 510(k) | K992211 | SPO2 WRAP SENSOR | DQA | 1999-12-22 | View |
| 510(k) | K990082 | EPIC SPO2 FINGER SENSOR, MODEL E403-09, E412-09 AND EPIC OXIMETER CABLE, MODEL E710-09 | DQA | 1999-04-09 | View |
| 510(k) | K970098 | E100 SERIES SPO2 SENSORS | DQA | 1998-04-30 | View |
| 510(k) | K965172 | OXIMETER PRE-AMP CABLE | DQA | 1997-07-16 | View |
| 510(k) | K964055 | FLEXI-SITE (E203-01)/ FLEXI-FIT (E300) | DQA | 1997-02-21 | View |
| 510(k) | K954168 | E100A PULSE OXIMETER FINGER SENSOR/PROBE | DQA | 1996-09-12 | View |
No matching devices.
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