Rehabilicare, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K022405 | MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MIC | GZJ | 2002-08-12 | View |
| 510(k) | K011017 | PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT | GZJ | 2001-09-24 | View |
| 510(k) | K982410 | SMP-PLUS,SX-PLUS,SX MODEL # 49XX SERIES 9 VOLT TENS DEVICE | GZJ | 1998-11-06 | View |
| 510(k) | K971542 | ORTHO DX NEUROMUSCULAR STIMULATOR | IPF | 1997-08-14 | View |
No matching devices.
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