This page includes the latest FDA filings for Concord Portex. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
CONCORD/PORTEX | STERI-CATH MDI | 1993-10-25 |
CONCORD/PORTEX | SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES | 1993-07-27 |
CONCORD/PORTEX | EPIDURAL MINIPACK | 1993-07-09 |
CONCORD/PORTEX | DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS | 1993-06-22 |
CONCORD/PORTEX | NEEDLE-PRO CARTRIDGE | 1993-04-29 |
CONCORD/PORTEX | HEAT MOISTURE CONDENSER | 1993-01-26 |
CONCORD/PORTEX | LOW PROFILE TRACHEOSTOMY TUBE | 1992-09-02 |
CONCORD/PORTEX | VACU-PRO | 1992-08-12 |
CONCORD/PORTEX | ANESTHESIA BREATHING CIRCUIT | 1992-02-14 |
CONCORD/PORTEX | NEW-VENT | 1991-08-26 |
CONCORD/PORTEX | TRACHEOSTOMY TUBE AND CUFF | 1991-08-16 |
CONCORD/PORTEX | ACCU-VENT(TM) WITH NEEDLE-PRO(TM) | 1991-07-05 |
CONCORD/PORTEX | SYRINGE TIP CAP | 1991-06-21 |
CONCORD/PORTEX | SAFETY NEEDLE SHEATH, MODIFICATION | 1991-05-03 |
CONCORD/PORTEX | ORAL PHARYNGEAL CLEANSING DEVICE | 1991-01-31 |
CONCORD/PORTEX | SAFETY NEEDLE SHEATH | 1990-12-19 |
CONCORD/PORTEX | D.I.C. TRACHEOSTOMY TUBES & LARYNGECTOMY TUBES | 1990-09-25 |
CONCORD/PORTEX | STERI-CATH-DL | 1990-08-29 |
CONCORD/PORTEX | MODIFIED ENDOBRONCHIAL TUBE | 1990-08-03 |
CONCORD/PORTEX | STERI-CATH(TM) | 1990-07-12 |
CONCORD/PORTEX | AMNIOTIC FLUID SAMPLER (AMNIOCENTESIS TRAY) | 1990-01-12 |
CONCORD/PORTEX | ANESTHESIA/RESPIRATORY DISPOSABLE MASK | 1989-08-21 |
CONCORD/PORTEX | SUCTION CONTROL VALVE | 1989-04-24 |