Caradyne, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K040862GUARDIAN NEONATE CPAP/HUMIDIFICATION SYSTEMJune 30, 2004
K023565OXICHECKMarch 28, 2003
K000959CRITERION 60 OR PM 60June 22, 2000
K992101CRITERION 40 OR PM 40January 6, 2000
K982283WHISPERFLOW OXYGEN FLOW GENERATOR - ADJUSTABLE MODEL WF 8500 WHISPERFLOW OXYGEN FLOW GENERATOR - FIXMarch 9, 1999