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NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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