FDA 510(k) Applications Submitted by CLAY ANSELMO

FDA 510(k) Number Submission Date Device Name Applicant
K120164 01/19/2012 PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE ANGIOSLIDE, LTD
K110499 02/22/2011 CG-5108 ACT-3L CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR CARD GUARD SCIENTIFIC SURVIVAL LTD.
K130524 02/28/2013 BREATHID HP SYSTEM EXALENZ BIOSCIENCE LTD.
K120805 03/16/2012 PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE ANGIOSLIDE, LTD
K071473 05/29/2007 MODIFICATION TO SUPERDIMENSION/BRONCHUS PREMIUM 2 SUPERDIMENSION, LTD.
K101639 06/10/2010 CG-6108 ACT-IL CONTINUOUS ECG MONITOR AND ARRYTHMIA DETECTOR CARD GUARD SCIENTIFIC SURVIVAL, LTD.
K111745 06/21/2011 KING OF HEARTS EXPRESS AF CARDIAC EVENT RECORDER CARD GUARD SCIENTIFIC SURVIVAL, LTD.
K111750 06/22/2011 EXTRA PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE; PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE ANGIOSLIDE, LTD
K051816 07/05/2005 LUMIWAVE 1X4 INFRARED THERAPY DEVICE BIOCARE SYSTEMS, INC.
K102199 08/04/2010 OTOMAG BONE CONDUCTION HEARING SYSTEM MODEL ALPHA 1 (S) AND ALPHA 1 (M) SOPHONO, INC
K042532 09/17/2004 BIOCARE SYSTEMS PREMIR 818 BIOCARE SYSTEMS, INC.
K133043 09/26/2013 PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE ANGIOSLIDE, LTD
K123426 11/07/2012 MEDICVOD, MEDICAST, MEDISHOW, MEDISEARCH, CENTRAL STORAGE SYSTEM - CSS ORPHEUS MEDICAL, LTD.
K023942 11/26/2002 CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311 YAMATO CORP.
K063753 12/19/2006 GFX NERVE ABLATION SYSTEM ACI, INC.


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