Southmedic, Inc. is one of 500 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Southmedic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Oxy2Pro, CO2/O2 NASAL CANNULA (WITH 4 (10CM) O2 AND CO2 TUBE), CO2/O2 NASAL CANNULA (WITH 8 (240CM) O2 AND 4 (10CM) CO2 TUBE),, SMDIA-1000
10
Total
10
Cleared
0
Denied
Southmedic, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Ancaster, Ontario, CA.
Last cleared in 2023. Active since 1984.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Southmedic, Inc.
10 devices
Cleared
Nov 21, 2023
Oxy2Pro
Anesthesiology
459d
Cleared
Jan 13, 2014
CO2/O2 NASAL CANNULA (WITH 4 (10CM) O2 AND CO2 TUBE), CO2/O2 NASAL CANNULA...
Anesthesiology
243d
Cleared
Jan 07, 2011
SMDIA-1000
Anesthesiology
179d
Cleared
Jun 11, 2002
OXYARM CO2
Anesthesiology
172d
Cleared
Feb 22, 1995
VAPOFIL
Anesthesiology
96d
Cleared
Mar 18, 1993
FUNNEL ADAPTOR
Anesthesiology
259d
Cleared
Sep 11, 1986
AEROSOL-T
Anesthesiology
16d
Cleared
May 21, 1986
VAPOFIL
Anesthesiology
8d
Cleared
Apr 17, 1986
VAPORIZER SPACER
Anesthesiology
63d
Cleared
Nov 15, 1984
ANAESLOCK THREE VAPORIZER INTERLOCK HVA003
Anesthesiology
35d