Concord/Portex - FDA 510(k) Cleared Devices
23
Total
20
Cleared
0
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.
23 devices
Cleared
Oct 25, 1993
STERI-CATH MDI
Anesthesiology
465d
Cleared
Jul 27, 1993
SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
General Hospital
193d
Cleared
Jul 09, 1993
EPIDURAL MINIPACK
Anesthesiology
304d
Cleared
Jun 22, 1993
DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS
Anesthesiology
152d
Cleared
Apr 29, 1993
NEEDLE-PRO CARTRIDGE
General Hospital
307d
Cleared
Jan 26, 1993
HEAT MOISTURE CONDENSER
Anesthesiology
175d
Cleared
Sep 02, 1992
LOW PROFILE TRACHEOSTOMY TUBE
Anesthesiology
86d
Cleared
Aug 12, 1992
VACU-PRO
Chemistry
82d
Cleared
Feb 14, 1992
ANESTHESIA BREATHING CIRCUIT
Anesthesiology
71d
Cleared
Aug 26, 1991
NEW-VENT
Chemistry
125d
Cleared
Aug 16, 1991
TRACHEOSTOMY TUBE AND CUFF
Anesthesiology
95d
Cleared
Jul 05, 1991
ACCU-VENT(TM) WITH NEEDLE-PRO(TM)
Anesthesiology
58d
Cleared
Jun 21, 1991
SYRINGE TIP CAP
Chemistry
71d
Cleared
May 03, 1991
SAFETY NEEDLE SHEATH, MODIFICATION
General Hospital
63d
Cleared
Jan 31, 1991
ORAL PHARYNGEAL CLEANSING DEVICE
Dental
85d
Cleared
Dec 19, 1990
SAFETY NEEDLE SHEATH
General Hospital
98d
Cleared
Sep 25, 1990
D.I.C. TRACHEOSTOMY TUBES & LARYNGECTOMY TUBES
Anesthesiology
40d
Cleared
Aug 29, 1990
STERI-CATH-DL
Anesthesiology
71d
Cleared
Aug 03, 1990
MODIFIED ENDOBRONCHIAL TUBE
Anesthesiology
85d
Cleared
Jul 12, 1990
STERI-CATH(TM)
Anesthesiology
43d
Cleared
Jan 12, 1990
AMNIOTIC FLUID SAMPLER (AMNIOCENTESIS TRAY)
Obstetrics & Gynecology
88d
Cleared
Aug 21, 1989
ANESTHESIA/RESPIRATORY DISPOSABLE MASK
Anesthesiology
161d
Cleared
Apr 24, 1989
SUCTION CONTROL VALVE
Anesthesiology
19d