Medical Device Manufacturer · CA , Ancaster, Ontario

Southmedic, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1984

Total

Cleared

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) cleared devices by Southmedic, Inc.

10 devices

1-10 of 10

Cleared Nov 21, 2023

Oxy2Pro

K222511 · CCK

Anesthesiology · 459d

Cleared Jan 13, 2014

CO2/O2 NASAL CANNULA (WITH 4 (10CM) O2 AND CO2 TUBE), CO2/O2 NASAL CANNULA...

K131410 · CCK

Anesthesiology · 243d

Cleared Jan 07, 2011

SMDIA-1000

K101953 · CAF

Anesthesiology · 179d

Cleared Jun 11, 2002

OXYARM CO2

K014211 · CCK

Anesthesiology · 172d

Anesthesiology · 259d

ANAESLOCK THREE VAPORIZER INTERLOCK HVA003

K843993 · CAD

Anesthesiology · 35d

Southmedic, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Southmedic, Inc.

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