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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