Neoforce Group, Inc.

Neoforce Group, Inc. holds 7 FDA 510(k) medical device clearances, first cleared 2006, most recent 2011.

Top product codes for Neoforce Group, Inc.

Recent clearances by Neoforce Group, Inc.

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

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