Back IN Action, 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) | K891458 | SW 803 LOW FREQUENCY STIMULATOR DANA TOUCH | IPF | 1989-10-20 | View |
| 510(k) | K891394 | PM830 ELECTRIC MASSAGER | ISA | 1989-04-10 | View |
No matching devices.
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