Pegasus Research Corp.

FDA Regulatory Profile

Pegasus Research Corp. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Nov 7, 2012.

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K122857HOPE CONTINUOUS NEBULIZER MODEL HOPE-11310, HEART NEBULIZER MODEL HEART-100609, THERAMIST NEBULIZER Nov 7, 2012
K020700PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPYApr 26, 2004
K013856PMH 1000 HEATED HUMIDIFIERFeb 21, 2003
K983783HEATED HUMIDIFIEROct 24, 2000
K962534THERA-MIST NEBULIZER MODEL-P3000Feb 28, 1997
K946057AQUALARM MOISTURE SENSOR MODEL P85000May 5, 1995
K915890AUTOCLAVABLE THERA-MIST HUMIDIFIER P3600, MODIFIEDJun 24, 1992
K914465AUTOCLAVABLE VERSION THERA-MIST NEBULIZER, P32000Mar 31, 1992
K903489THERA-MIST TM VOLUMINA INCENT SPIROMETER, P40000Dec 10, 1990
K894000THERA-MIST HUMIDIFIERAug 28, 1989
K893942THERA-MIST(TM) NEBULIZER, MODEL 30000Aug 28, 1989
K880473AERO-MIST NEBULIZER HEATERMar 31, 1988