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geko T-2 and geko T-3 Neuromuscular Stimulators

Page Type
Cleared 510(K)
510(k) Number
K191113
510(k) Type
Traditional
Applicant
Firstkind Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/18/2019
Days to Decision
145 days
Submission Type
Summary

geko T-2 and geko T-3 Neuromuscular Stimulators

Page Type
Cleared 510(K)
510(k) Number
K191113
510(k) Type
Traditional
Applicant
Firstkind Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/18/2019
Days to Decision
145 days
Submission Type
Summary