Concord/Portex
Concord/Portex holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1993.
Top product codes for Concord/Portex
Recent clearances by Concord/Portex
- K923559 — STERI-CATH MDI
- K930218 — SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
- K924541 — EPIDURAL MINIPACK
- K930286 — DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS
- K923127 — NEEDLE-PRO CARTRIDGE
- K923910 — HEAT MOISTURE CONDENSER
- K922749 — LOW PROFILE TRACHEOSTOMY TUBE
- K922445 — VACU-PRO
- K915452 — ANESTHESIA BREATHING CIRCUIT
- K911809 — NEW-VENT
- K912124 — TRACHEOSTOMY TUBE AND CUFF
- K912043 — ACCU-VENT(TM) WITH NEEDLE-PRO(TM)
- K911638 — SYRINGE TIP CAP
- K911037 — SAFETY NEEDLE SHEATH, MODIFICATION
- K905011 — ORAL PHARYNGEAL CLEANSING DEVICE
- K904198 — SAFETY NEEDLE SHEATH
- K903730 — D.I.C. TRACHEOSTOMY TUBES & LARYNGECTOMY TUBES
- K902687 — STERI-CATH-DL
- K902116 — MODIFIED ENDOBRONCHIAL TUBE
- K902383 — STERI-CATH(TM)
- K896031 — AMNIOTIC FLUID SAMPLER (AMNIOCENTESIS TRAY)
- K891316 — ANESTHESIA/RESPIRATORY DISPOSABLE MASK
- K892343 — SUCTION CONTROL VALVE
Data sourced from openFDA. This site is unofficial and independent of the FDA.