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FDA 510(k) Applications Submitted by FIRSTKIND LIMITED
FDA 510(k) Number
Submission Date
Device Name
Applicant
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
K133638
11/27/2013
GEKO
FIRSTKIND LIMITED
K134001
12/27/2013
FIREFLY
FIRSTKIND LIMITED
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