FDA 510(k) Applications Submitted by Cherita James

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130114	01/16/2013	PAINMASTER MCT PATCH	NEWMARK, INC.
K060471	02/23/2006	FSSB NYLON SURGICAL SUTURES	FSSB CHIRURGISCHE NADELN GMBH
K090452	02/23/2009	NEOSS IMPLANT SYSTEM 03.25	NEOSS LTD
K140467	02/24/2014	FLEX-MT +	EMSI
K060708	03/16/2006	SOMNOSCREEN	SOMNOMEDICS GMBH & CO. KG
K090717	03/18/2009	FLEX-TENS	EMSI
K090889	03/31/2009	EMSI GARMENT ELECTRODES	EMSI
K111347	05/13/2011	ISROBOT MONA LISA	BIOBOT SURGICAL PTE LTD
K081485	05/28/2008	SOMNOWATCH	SOMNOMEDICS GMBH
K071556	06/07/2007	SOMNOSCREEN EEG10-20	SOMNOMEDICS GMBH
K132044	07/02/2013	CRANIAL LOOP, CRANIAL LOOP L AND CRANIAL LOOP XL AND CRANIAL BONE FIXATION SYSTEM	NEOS SURGERY S.L.
K071869	07/06/2007	TENS/IF 14	EMSI
K062081	07/21/2006	LITHOGOLD	TISSUE REGENERATION TECHNOLOGIES, INC.
K132401	08/01/2013	MEGA ISQ	OSSTELL AB
K102202	08/04/2010	GS 3000	EMSI
K082523	09/02/2008	OSSTELL ISQ IMPLANT STABILITY METER	OSSTELL AB
K083030	10/10/2008	TENS-EMS-14	EMSI
K093499	11/12/2009	HAIRMAX LASERCOMB	LEXINGTON INTERNATIONAL, LLC
K113376	11/16/2011	NEOSS PROACTIVE TAPERED IMPLANT	NEOSS LTD
K193307	11/29/2019	HIP7	Brainlab AG
K083561	12/02/2008	NEOSS PROACTIVE IMPLANT	NEOSS, LTD.
K083630	12/08/2008	CLUE MEDICAL AND CLUE MEDICAL BASIC	TELOVITAL GMBH TELEMEDIZIN