A Plus Medical is one of 18333 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A Plus Medical - FDA 510(k) Cleared Devices
Recent clearances: BABI PLUS NEONATAL RESUSCITATION BAG, BABI PLUS INFANT NASAL CANNULA SYSTEM, BABI*PLUS PRESSURE RELIEF MANIFOLD - 10CM H20, 12.5CM H20, 15CM H20
7
Total
7
Cleared
0
Denied
A Plus Medical has 7 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 7 cleared submissions from 2009 to 2012. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by A Plus Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A Plus Medical
7 devices
Cleared
Jan 13, 2012
BABI PLUS NEONATAL RESUSCITATION BAG
Anesthesiology
87d
Cleared
Oct 07, 2011
BABI PLUS INFANT NASAL CANNULA SYSTEM
Anesthesiology
231d
Cleared
Aug 01, 2011
BABI*PLUS PRESSURE RELIEF MANIFOLD - 10CM H20, 12.5CM H20, 15CM H20
Anesthesiology
172d
Cleared
Nov 18, 2010
VENTIPLUS DISPOSABLE MANOMETER 0-60 CM H2O
Anesthesiology
90d
Cleared
May 13, 2010
BABI PLUS INFANT NASAL CANNULA SYSTEM
Anesthesiology
162d
Cleared
Nov 23, 2009
VENTI.PLUS HYPERINFLATION BAG SYSTEM WITH PRESSURE MANOMETER
Anesthesiology
83d
Cleared
May 20, 2009
BABI*PLUS BUBBLE PAP VALVE
Anesthesiology
100d