Ceramatec, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K972992 | CERAMATEC MAXCELL AND CAG GALVANIC OXYGEN SENSORS | CCL | 1998-03-30 | View |
| 510(k) | K973282 | HANDI OXYGEN ANALYZER | CCL | 1998-03-04 | View |
| 510(k) | K911344 | CERION HAND HELD OXYGEN ANALYZER | CCL | 1991-06-18 | View |
| 510(k) | K880448 | CERION OXY THRESHOLD ALARM | CCL | 1988-03-21 | View |
No matching devices.
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