FDA 510(k) Applications Submitted by NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS

FDA 510(k) Number Submission Date Device Name Applicant
K080219 01/29/2008 MODIFICATION TO:NESS L300 NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
K031900 06/19/2003 HANDMASTER NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
K012823 08/16/2001 MODIFICATION TO HANDMASTER NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
K022776 08/21/2002 NESS SYSTEM NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
K024279 12/23/2002 NESS CHILDREN SYSTEM NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
K053468 12/13/2005 NESS L300 NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
K111767 06/23/2011 NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS


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