FDA 510(k) Applications Submitted by Rhythmlink International, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K022914 09/03/2002 RHYTHMLINK INTERNATIONAL SUBDERMAL NEEDLE ELECTRODES RHYTHMLINK INTERNATIONAL, LLC
K172503 08/18/2017 MR Conditional Cup Electrode, MR Conditional Webb Electrode Rhythmlink International, LLC
K190801 03/29/2019 PressOn Electrode Headset Rhythmlink International, LLC
K200984 04/14/2020 Guardian Needle Electrode Rhythmlink International, LLC
K191225 05/07/2019 EEG Electrode Template Rhythmlink International, LLC
K203079 10/13/2020 MR Conditional Sticky Pad Electrode Rhythmlink International, LLC
K120342 02/03/2012 EMG RECORDING ELECTRODE ASSEMBLY RHYTHMLINK INTERNATIONAL, LLC
K121347 05/01/2012 PRESSON ELECTRODE RHYTHMLINK INTERNATIONAL, LLC
K112435 08/24/2011 RHYTHMLINK MONOPOLAR STIMULATING INSTRUMENT RHYTHMLINK INTERNATIONAL, LLC
K072736 09/27/2007 RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT RHYTHMLINK INTERNATIONAL, LLC
K130220 01/29/2013 MR CONDITIONAL PRESSON ELECTRODE RHYTHMLINK INTERNATIONAL, LLC
K130287 02/05/2013 MR CONDITIONAL CUP ELECTRODE, MR CONDITIONAL WEBB ELECTRODE RHYTHMLINK INTERNATIONAL, LLC
K091055 04/13/2009 RHYTHMLINK DISPOSABLE CONCENTRIC EMG NEEDLE, MODEL D039032252R RHYTHMLINK INTERNATIONAL, LLC
K091056 04/13/2009 RHYTHMLINK DISPOSABLE MONOPOLAR EMG NEEDLE, MODEL TFDN26032252R RHYTHMLINK INTERNATIONAL, LLC
K132138 07/11/2013 RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE RHYTHMLINK INTERNATIONAL, LLC
K052188 08/11/2005 CUTANEOUS ELECTRODE RHYTHMLINK INTERNATIONAL, LLC
K103200 11/01/2010 PROPEP DELIVERY DEVICE RHYTHMLINK INTERNATIONAL, LLC
K061148 04/25/2006 RHYTHMLINK DISC ELECTRODES RHYTHMLINK INTERNATIONAL, LLC


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