FDA 510(k) Applications Submitted by Theron Gober
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K120862 |
03/22/2012 |
WATER BOTTLE CAP IRRIGATON SYSTEM |
ENDOCHOICE, INC. |
K080959 |
04/03/2008 |
DORNIER MEDILAS D 30 LASER, MEDILAS D 1064 |
DORNIER MEDTECH AMERICA, INC. |
K200986 |
04/15/2020 |
OPTI« B-Lac Cassette |
OPTI Medical Systems, Inc. |
K101298 |
05/10/2010 |
ENDOCHOICE GRASPING INSULATED AND ALIGATOR JAW FORCEPS MODEL AMHGFA, ENDOCHOICE GRASPING INSULATED AND RAT TOOTH FORCEPS |
ENDOCHOICE, INC. |
K151475 |
06/02/2015 |
EndoChoice Select Injection Needle |
ENDOCHOICE, INC. |
K111821 |
06/28/2011 |
BIOPSY VALVE |
ENDOCHOICE, INC. |
K132065 |
07/03/2013 |
INJECTION NEEDLE |
ENDOCHOICE, INC. |
K112576 |
09/06/2011 |
ENDOCHOICE WATER BOTTLE CAP SYSTEM |
ENDOCHOICE, INC. |
K083258 |
11/04/2008 |
MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE |
DORNIER MEDTECH AMERICA, INC. |
K083500 |
11/25/2008 |
MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE |
DORNIER MEDTECH AMERICA, INC. |
K073427 |
12/06/2007 |
MEDILAS D FAMILY LASERS |
DORNIER MEDTECH AMERICA, INC. |
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