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Rehabilicare, Inc.

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MIC (K022405)Rehabilicare, Inc.2002-08-12
PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT (K011017)Rehabilicare, Inc.2001-09-24
SMP-PLUS,SX-PLUS,SX MODEL # 49XX SERIES 9 VOLT TENS DEVICE (K982410)Rehabilicare, Inc.1998-11-06
ORTHO DX NEUROMUSCULAR STIMULATOR (K971542)Rehabilicare, Inc.1997-08-14

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Every clearance here is in the API, with alerts when new ones post.