FDA 510(k) Applications Submitted by SANJAY PARIKH

FDA 510(k) Number Submission Date Device Name Applicant
K100129 01/19/2010 AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO X AMBU A/S
K010583 02/27/2001 AMBU GEL, HYDROGEL BURN DRESSING AMBU, INC.
K130845 03/26/2013 AMBU ASCOPE 3 5.0/2.2; AMBU ASCOPE 3 SLIM 3.8/1.2; AMBU AVIEW AMBU A/S
K110962 04/06/2011 AMBU ASCOPE 2 AMBU A/S
K040991 04/16/2004 AMBU DISPOSABLE PRESSURE MANOMETER AMBU, INC.
K041026 04/21/2004 AMBU BLUE SENSOR, MRX, ECG ELECTRODE PRODUCT #:MRX-00-S AMBU, INC.
K071185 04/30/2007 MODIFICATION TO: AMBU NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODE AMBU A/S
K071186 04/30/2007 MODIFICATION TO: AMBU NEUROLINE CONCENTRIC NEEDLE ELECTRODE AMBU A/S
K051529 06/09/2005 AMBU NEUROLINE GROUND AMBU, INC.
K041734 06/25/2004 AMBU DISPOSABLE ECG ELECTRODE AMBU, INC.
K032278 07/24/2003 AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE AMBU, INC.
K982722 08/05/1998 AMBU MEDIBAG ADULT, AMBU MEDIBAG INFANT/CHILD AMBU, INC.
K032421 08/05/2003 AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE AMBU, INC.
K992902 08/30/1999 AMBU HAND POWER SUCTION PUMP AMBU, INC.
K042682 09/29/2004 AMBU SPUR II. ADULT SINGLE PATIENT RESUSCITATOR AMBU, INC.
K102824 09/29/2010 AMBU OVAL SILICONE RESUSCITATOR, ADULT AND PEDIATRIC AMBU A/S
K993278 09/30/1999 AMBU NEONATE SILICONE RESUSCITATOR AMBU, INC.
K093186 10/09/2009 AMBU ASCOPE AND MONITOR AMBU A/S
K042843 10/14/2004 AMBU SPUR II INFANT AND PEDIATRIC SINGLE PATIENT USE RESUSCITATORS AMBU, INC.
K052944 10/20/2005 AMBU WHITE SENSOR CFM, CFL AMBU A/S
K053140 11/09/2005 AMBU MARK IV RESUSCITATOR AMBU A/S
K053142 11/09/2005 AMBU MARK IV BABY RESUSCITATOR AMBU A/S
K093825 12/14/2009 AMBU NEUROLINE DISPOSABLE INOJECT NEEDLE ELECTRODE AMBU A/S
K053550 12/20/2005 AMBU BLUE SENSOR NEO AND NEO X AMBU A/S
K981891 05/29/1998 AMBU TUBECHECK AMBU, INC.
K964584 11/15/1996 AMBU SPUR NEONATE AMBU, INC.


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