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geko(TM) Plus R-2 Neuromuscular Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160299
510(k) Type
Special
Applicant
FIRSTKIND LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/8/2016
Days to Decision
64 days
Submission Type
Summary

geko(TM) Plus R-2 Neuromuscular Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160299
510(k) Type
Special
Applicant
FIRSTKIND LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/8/2016
Days to Decision
64 days
Submission Type
Summary