Medical Device Manufacturer · US , New Brighton , MN

Rehabilicare, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1997

Recent clearances: MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE, PROMAX-XP, TENS AND MICROCURRENT DEVICE, SMP-PLUS,SX-PLUS,SX MODEL # 49XX SERIES 9 VOLT TENS DEVICE

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Rehabilicare, Inc. Neurology ✕

3 devices

1-3 of 3

Cleared Aug 12, 2002

MODIFICATION TO PROMAX-XP, TENS AND MICROCURRENT DEVICE

Neurology · 27d

Cleared Sep 24, 2001

PROMAX-XP, TENS AND MICROCURRENT DEVICE

Neurology · 173d

Cleared Nov 06, 1998

SMP-PLUS,SX-PLUS,SX MODEL # 49XX SERIES 9 VOLT TENS DEVICE

Neurology · 116d