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NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT

Page Type
Cleared 510(K)
510(k) Number
K111767
510(k) Type
Traditional
Applicant
NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/15/2011
Days to Decision
84 days
Submission Type
Statement

NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT

Page Type
Cleared 510(K)
510(k) Number
K111767
510(k) Type
Traditional
Applicant
NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/15/2011
Days to Decision
84 days
Submission Type
Statement