Rabar, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K844017 | MICROTENS 7757 T.E.N.S. STIMULATOR | GFJ | 1984-11-30 | View |
| 510(k) | K842414 | ECHO PULSE BURST | GZJ | 1984-07-27 | View |
| 510(k) | K821736 | ECHO-PULSE KM555 | GXW | 1982-12-09 | View |
No matching devices.
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