Amplaid USA, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K861014 | AMPLAID MK15 (EVOKED POTENTIAL SYSTEM) | GWL | 1986-08-20 | View |
| 510(k) | K832510 | EVOKED POTENTIALS SYSTEM MK10 | GWJ | 1983-11-25 | View |
| 510(k) | K810482 | SOMATOSENSORY STIMULATOR | GWF | 1981-04-29 | View |
| 510(k) | K810473 | MK6 ERA SYSTEM | GWJ | 1981-04-29 | View |
| 510(k) | K810481 | VISUAL PATTERN REVERSAL GEN. & PHOTIC S. | GWE | 1981-03-11 | View |
| 510(k) | K802963 | 101, 151, 161 PORTABLE AUDIOMETERS | EWO | 1980-12-19 | View |
| 510(k) | K802097 | SELF-RECORDING ADMITTANCE METER 709 | ETY | 1980-10-10 | View |
| 510(k) | K781667 | AMPLAID MARK 4 AND MARK 5 | GWJ | 1978-11-03 | View |
No matching devices.
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