FDA 510(k) Applications Submitted by JAMES M MEWBORNE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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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