Medical Device Manufacturer · US , Keene , NH

Concord/Portex - FDA 510(k) Cleared Devices

23 submissions · 20 cleared · Since 1989

23

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Concord/Portex Anesthesiology ✕

14 devices

1-14 of 14

Cleared Oct 25, 1993

Anesthesiology · 465d

Cleared Jul 09, 1993

EPIDURAL MINIPACK

Anesthesiology · 304d

Cleared Jun 22, 1993

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS

Anesthesiology · 152d

Cleared Jan 26, 1993

HEAT MOISTURE CONDENSER

Anesthesiology · 175d

Cleared Sep 02, 1992

LOW PROFILE TRACHEOSTOMY TUBE

Anesthesiology · 86d

Cleared Feb 14, 1992

ANESTHESIA BREATHING CIRCUIT

Anesthesiology · 71d

Cleared Aug 16, 1991

TRACHEOSTOMY TUBE AND CUFF

Anesthesiology · 95d

Cleared Jul 05, 1991

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

Anesthesiology · 58d

Cleared Sep 25, 1990

D.I.C. TRACHEOSTOMY TUBES & LARYNGECTOMY TUBES

Anesthesiology · 40d

Cleared Aug 29, 1990

Anesthesiology · 71d

Cleared Aug 03, 1990

MODIFIED ENDOBRONCHIAL TUBE

Anesthesiology · 85d

Cleared Jul 12, 1990

Anesthesiology · 43d

Cleared Aug 21, 1989

ANESTHESIA/RESPIRATORY DISPOSABLE MASK

Anesthesiology · 161d

Cleared Apr 24, 1989

SUCTION CONTROL VALVE

Anesthesiology · 19d