Pegasus Research Corp. is one of 18347 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pegasus Research Corp. - FDA 510(k) Cleared Devices
Recent clearances: HOPE CONTINUOUS NEBULIZER MODEL HOPE-11310, HEART NEBULIZER MODEL HEART-100609, THERAMIST NEBULIZER MODEL THERAMIST-3100, PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY, PMH 1000 HEATED HUMIDIFIER
12
Total
12
Cleared
0
Denied
Pegasus Research Corp. has 12 FDA 510(k) cleared anesthesiology devices. Based in Corona Del Mar, US.
Historical record: 12 cleared submissions from 1988 to 2012.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pegasus Research Corp.
12 devices
Cleared
Nov 07, 2012
HOPE CONTINUOUS NEBULIZER MODEL HOPE-11310, HEART NEBULIZER MODEL...
Anesthesiology
50d
Cleared
Apr 26, 2004
PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY
Anesthesiology
784d
Cleared
Feb 21, 2003
PMH 1000 HEATED HUMIDIFIER
Anesthesiology
472d
Cleared
Oct 24, 2000
HEATED HUMIDIFIER
Anesthesiology
728d
Cleared
Feb 28, 1997
THERA-MIST NEBULIZER MODEL-P3000
Anesthesiology
245d
Cleared
May 05, 1995
AQUALARM MOISTURE SENSOR MODEL P85000
Anesthesiology
144d
Cleared
Jun 24, 1992
AUTOCLAVABLE THERA-MIST HUMIDIFIER P3600, MODIFIED
Anesthesiology
183d
Cleared
Mar 31, 1992
AUTOCLAVABLE VERSION THERA-MIST NEBULIZER, P32000
Anesthesiology
176d
Cleared
Dec 10, 1990
THERA-MIST TM VOLUMINA INCENT SPIROMETER, P40000
Anesthesiology
130d
Cleared
Aug 28, 1989
THERA-MIST(TM) NEBULIZER, MODEL 30000
Anesthesiology
89d
Cleared
Aug 28, 1989
THERA-MIST HUMIDIFIER
Anesthesiology
84d
Cleared
Mar 31, 1988
AERO-MIST NEBULIZER HEATER
Anesthesiology
56d