Respironics New Jersey, Inc. is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Respironics New Jersey, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OPTICHAMBER DIAMOND VALVED HOLDING CHAMBER, LITETOUCH MASK, OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER
5
Total
5
Cleared
0
Denied
Respironics New Jersey, Inc. has 5 FDA 510(k) cleared medical devices. Based in Cedar Grove, US.
Historical record: 5 cleared submissions from 2004 to 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Respironics New Jersey, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc., Entela, Inc. and Intertek Testing Services.
FDA 510(k) Regulatory Record - Respironics New Jersey, Inc.
5 devices
Cleared
Aug 09, 2011
OPTICHAMBER DIAMOND VALVED HOLDING CHAMBER
Anesthesiology
189d
Cleared
Jun 29, 2010
LITETOUCH MASK
Anesthesiology
148d
Cleared
Sep 12, 2007
OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER
Anesthesiology
15d
Cleared
Dec 20, 2005
MYNEB NEBULIZER, MODEL RDD100
Anesthesiology
34d
Cleared
Oct 13, 2004
INSPIRATION ELITE NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS456
Anesthesiology
15d