Medical Device Manufacturer · US , Keene , NH

Concord/Portex - FDA 510(k) Cleared Devices

23 submissions · 20 cleared · Since 1989

Total

Cleared

Denied

Concord/Portex has 20 FDA 510(k) cleared medical devices. Based in Keene, US.

Historical record: 20 cleared submissions from 1989 to 1993. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Concord/Portex Filter by specialty or product code using the sidebar.

Concord/Portex is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Concord/Portex

23 devices

1-12 of 23

Cleared Oct 25, 1993

STERI-CATH MDI

K923559 · CAF

Anesthesiology · 465d

Cleared Jul 27, 1993

SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES

K930218 · MAJ

General Hospital · 193d

Cleared Jul 09, 1993

EPIDURAL MINIPACK

K924541 · BYO

Anesthesiology · 304d

Cleared Jun 22, 1993

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS

K930286 · CBT

Anesthesiology · 152d

Cleared Apr 29, 1993

NEEDLE-PRO CARTRIDGE

K923127 · FMI

General Hospital · 307d

Cleared Jan 26, 1993

HEAT MOISTURE CONDENSER

K923910 · BYD

Anesthesiology · 175d

Cleared Sep 02, 1992

LOW PROFILE TRACHEOSTOMY TUBE

ANESTHESIA BREATHING CIRCUIT

TRACHEOSTOMY TUBE AND CUFF

K912124 · BTO

Anesthesiology · 95d

Cleared Jul 05, 1991

ACCU-VENT(TM) WITH NEEDLE-PRO(TM)

K912043 · CBT

Anesthesiology · 58d

Concord/Portex - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Concord/Portex

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