FDA 510(k) Applications Submitted by CURTIS JENSEN
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K060236 |
01/30/2006 |
MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE |
IOMED, INC. |
K140384 |
02/14/2014 |
FMWAND HANDPIECE SE |
DOMAIN SURGICAL, INC. |
K110439 |
02/15/2011 |
DOMAIN SURGICAL SYSTEM |
DOMAIN SURGICAL, INC. |
K130606 |
03/07/2013 |
FMWAND FERROMAGNETIC SURGICAL SYSTEM |
DOMAIN SURGICAL, INC. |
K031115 |
04/08/2003 |
RH-900 |
IOMED, INC. |
K091133 |
04/20/2009 |
APLION TOPICAL CARE SYSTEM |
APLION MEDICAL,LLC |
K141484 |
06/05/2014 |
OPEN FMSEALER |
DOMAIN SURGICAL, INC. |
K121881 |
06/26/2012 |
DOMAIN SURGICAL SYSTEM |
DOMAIN SURGICAL, INC. |
K142229 |
08/13/2014 |
Laparoscopic FMsealer |
DOMAIN SURGICAL, INC. |
K033192 |
10/02/2003 |
RH-950 |
IOMED, INC. |
K162771 |
10/03/2016 |
EkoSonic Endovascular System with Control Unit 4.0 |
BTG International, Inc. |
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