Rehabilicare, Inc.
Rehabilicare, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2002.
Top product codes for Rehabilicare, Inc.
Recent clearances by Rehabilicare, Inc.
- K022405 — MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MIC
- K011017 — PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT
- K982410 — SMP-PLUS,SX-PLUS,SX MODEL # 49XX SERIES 9 VOLT TENS DEVICE
- K971542 — ORTHO DX NEUROMUSCULAR STIMULATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.