Motion Lab Systems, 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) | K000220 | MA-300 ELECTROMYOGRAPHY SYSTEM | IKN | 2000-02-24 | View |
| 510(k) | K974385 | MLS ELECTROMYOGRAPHIC PREAMPLIFIER | IKN | 1998-02-19 | View |
No matching devices.
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