FDA 510(k) Applications Submitted by LAUREN R ZIEGLER

FDA 510(k) Number Submission Date Device Name Applicant
K100285 02/01/2010 LITETOUCH MASK RESPIRONICS NEW JERSEY, INC.
K110293 02/01/2011 OPTICHAMBER DIAMOND VALVED HOLDING CHAMBER RESPIRONICS NEW JERSEY, INC.
K072418 08/28/2007 OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER RESPIRONICS NEW JERSEY, INC.
K062689 09/11/2006 SIDESTREAM PLUS RESPIRONICS LTD.
K042655 09/28/2004 INSPIRATION ELITE NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS456 RESPIRONICS NEW JERSEY, INC.
K053203 11/16/2005 MYNEB NEBULIZER, MODEL RDD100 RESPIRONICS NEW JERSEY, INC.
K980951 03/13/1998 ONEFLOW STI MEDICAL
K961077 03/18/1996 PEP (POSITIVE EXPIRATORY PRESSURE) THERAPY DEVICE HEALTHSCAN PRODUCTS, INC.
K952909 06/23/1995 AUTOZONE HEALTHSCAN, INC.
K962822 07/19/1996 OPTICHAMBER HEALTHSCAN PRODUCTS, INC.
K962924 07/29/1996 PERSONAL BEST II WITH ZONE MANAGEMENT SYSTEM HEALTHSCAN PRODUCTS, INC.
K962929 07/29/1996 PERSONAL BEST II HEALTHSCAN PRODUCTS, INC.
K963793 09/23/1996 OPTIVENT HEALTHCARE PRODUCTS, INC.


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