Neoforce Group, Inc.

7 FDA 510(k) medical device clearances.

Top product codes for Neoforce Group, Inc.

Recent clearances by Neoforce Group, Inc.

K110119 — PRESSURE MANOMETER CAP · 2011-06-10
K103833 — NEOPIP PATIENT CIRCUIT WITH PEEP BYE · 2011-04-20
K102649 — NEOPOP INFANT RESUSCITATOR WITH FLOW METER BTM · 2011-01-06
K092085 — ISPIRA RESUSCITATION UNIT BTL · 2009-10-07
K072021 — NEOPIP INFANT RESUSCITATOR BTM · 2007-09-12
K070416 — NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP BYE · 2007-05-29
K061280 — V-2200 INFANT INCUBATOR FMZ · 2006-06-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.