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geko™ T-2 and geko™ Plus R-2 Neuromuscular Stimulators

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163125
510(k) Type
Traditional
Applicant
FIRSTKIND LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/10/2017
Days to Decision
153 days
Submission Type
Summary

geko™ T-2 and geko™ Plus R-2 Neuromuscular Stimulators

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163125
510(k) Type
Traditional
Applicant
FIRSTKIND LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/10/2017
Days to Decision
153 days
Submission Type
Summary