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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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