Neoforce Group, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K110119PRESSURE MANOMETERJune 10, 2011
K103833NEOPIP PATIENT CIRCUIT WITH PEEPApril 20, 2011
K102649NEOPOP INFANT RESUSCITATOR WITH FLOW METERJanuary 6, 2011
K092085ISPIRA RESUSCITATION UNITOctober 7, 2009
K072021NEOPIP INFANT RESUSCITATORSeptember 12, 2007
K070416NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEPMay 29, 2007
K061280V-2200 INFANT INCUBATORJune 27, 2006