Portex, Inc. is one of 5539 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Portex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETER, PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT, 1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
20
Total
20
Cleared
0
Denied
Portex, Inc. has 20 FDA 510(k) cleared anesthesiology devices. Based in Walker, US.
Historical record: 20 cleared submissions from 1977 to 2004.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Portex, Inc.
20 devices
Cleared
Mar 10, 2004
PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETER
Anesthesiology
163d
Cleared
Jul 18, 2003
PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT
Anesthesiology
106d
Cleared
Feb 11, 2003
1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
Anesthesiology
90d
Cleared
Feb 27, 2002
1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX
Anesthesiology
75d
Cleared
Feb 13, 2002
HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE
General Hospital
65d
Cleared
Mar 24, 1988
LARYNGECTOMY TUBE
Ear, Nose, Throat
175d
Cleared
Jan 19, 1988
THERMOVENT 600, 1200, T, 02
Anesthesiology
71d
Cleared
Aug 06, 1986
MINI-TRACH KIT
Anesthesiology
58d
Cleared
Jul 06, 1984
JET VENTILATION ADAPTOR
Cardiovascular
14d
Cleared
Feb 04, 1984
IRRI-CATH
Anesthesiology
82d
Cleared
Jan 17, 1984
ENDOBRONCHIAL TWIN LUMEN TUBE
Anesthesiology
20d
Cleared
Jan 17, 1984
SWIVEL ADAPTOR W/ALARM PORT
Anesthesiology
13d