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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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