Lamont Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042364 | PANBUS DIGITAL EEG & SLEEP ACQUISITION DEVICES | OLV | 2004-09-30 | View |
| 510(k) | K990522 | WARATAH DIGITAL EEG AND SLEEP ACQUISITION DEVICES WITH, OR WITHOUT, PULSE OXIMETRY,CARDINAL DIGITAL EEG AND SLEEP ACQUIS | OLV | 1999-05-19 | View |
No matching devices.
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