Portex, Inc.
Portex, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2004.
Top product codes for Portex, Inc.
Recent clearances by Portex, Inc.
- K033080 — PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETER
- K031057 — PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT
- K023793 — 1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
- K014115 — 1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX
- K014073 — HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE
- K873992 — LARYNGECTOMY TUBE
- K874597 — THERMOVENT 600, 1200, T, 02
- K862167 — MINI-TRACH KIT
- K842456 — JET VENTILATION ADAPTOR
- K833908 — IRRI-CATH
- K834565 — ENDOBRONCHIAL TWIN LUMEN TUBE
- K840015 — SWIVEL ADAPTOR W/ALARM PORT
- K833189 — HYDROFLOW SUCTION IRRIGATION SYSTEM
- K830716 — CARDIO-ESOPHASCOPE
- K830352 — REINFORCED SILICONE TRACHEAL TUBE
- K810147 — ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE
- K802065 — CONTINUOUS EPIDURAL ANESTHESIA TRAY/DRUG
- K792202 — TROCAR CATHETER/THORACIC CATHETER
- K781052 — CONTINUOUS EPIDURAL ANESTHESIA TRAY
- K770112 — SPECIMEN COLLECTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.