Rhythmlink International, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rhythmlink International, LLC - FDA 510(k) Cleared Devices
Recent clearances: MR Conditional Sticky Pad Electrode, Guardian Needle Electrode, EEG Electrode Template
18
Total
18
Cleared
0
Denied
Rhythmlink International, LLC has 18 FDA 510(k) cleared neurology devices. Based in Cayce, US.
Last cleared in 2021. Active since 2002.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rhythmlink International, LLC
18 devices
Cleared
Feb 09, 2021
MR Conditional Sticky Pad Electrode
Neurology
119d
Cleared
May 27, 2020
Guardian Needle Electrode
Neurology
43d
Cleared
Aug 05, 2019
EEG Electrode Template
Neurology
90d
Cleared
Jul 10, 2019
PressOn Electrode Headset
Neurology
103d
Cleared
Dec 01, 2017
MR Conditional Cup Electrode, MR Conditional Webb Electrode
Neurology
105d
Cleared
Apr 11, 2014
RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE
Neurology
274d
Cleared
Jul 22, 2013
MR CONDITIONAL PRESSON ELECTRODE
Neurology
174d
Cleared
May 30, 2013
MR CONDITIONAL CUP ELECTRODE, MR CONDITIONAL WEBB ELECTRODE
Neurology
114d
Cleared
Jul 12, 2012
PRESSON ELECTRODE
Neurology
72d
Cleared
Jun 22, 2012
EMG RECORDING ELECTRODE ASSEMBLY
Neurology
140d
Cleared
Sep 22, 2011
RHYTHMLINK MONOPOLAR STIMULATING INSTRUMENT
Ear, Nose, Throat
29d
Cleared
Apr 12, 2011
PROPEP DELIVERY DEVICE
General Hospital
162d