FDA 510(k) Applications Submitted by NEOFORCE GROUP, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K070416 02/12/2007 NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP NEOFORCE GROUP, INC.
K061280 05/08/2006 V-2200 INFANT INCUBATOR NEOFORCE GROUP, INC.
K092085 07/09/2009 ISPIRA RESUSCITATION UNIT NEOFORCE GROUP, INC.
K072021 07/23/2007 NEOPIP INFANT RESUSCITATOR NEOFORCE GROUP, INC.
K102649 09/14/2010 NEOPOP INFANT RESUSCITATOR WITH FLOW METER NEOFORCE GROUP, INC.
K103833 12/30/2010 NEOPIP PATIENT CIRCUIT WITH PEEP NEOFORCE GROUP, INC.


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