FDA 510(k) Applications Submitted by NEIL BUCKLEY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180082	01/11/2018	geko T-2 and geko Plus R-2	Firstkind Ltd
K160299	02/04/2016	geko(TM) Plus R-2 Neuromuscular Stimulator	FIRSTKIND LIMITED
K220327	02/04/2022	geko W-3	Firstkind Limited
K181059	04/23/2018	geko T-3 Neuromuscular Stimulator	Firstkind Limited
K191113	04/26/2019	geko T-2 and geko T-3 Neuromuscular Stimulators	Firstkind Limited
K201131	04/28/2020	firefly T-2	Firstkind Limited
K212762	08/31/2021	geko W-2	Firstkind Limited
K152677	09/18/2015	geko T-2 Neuromuscular Stimulator	FIRSTKIND LIMITED
K193045	11/01/2019	gekoÖ W-2	Firstkind Limited
K163125	11/08/2016	gekoÖ T-2 and gekoÖ Plus R-2 Neuromuscular Stimulators	FIRSTKIND LIMITED