Last synced on 25 January 2026 at 3:41 am

HANDMASTER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010837
510(k) Type
Traditional
Applicant
Neuromusclar Electrical Stimulation Systems, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
87 days
Submission Type
Summary

HANDMASTER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010837
510(k) Type
Traditional
Applicant
Neuromusclar Electrical Stimulation Systems, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
87 days
Submission Type
Summary