Medical Device Manufacturer · US , Walker , MI

Portex, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1977

Total

Cleared

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

1-12 of 20

Cleared Mar 10, 2004

PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETER

K033080 · CAZ

Anesthesiology · 163d

Cleared Jul 18, 2003

PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT

K031057 · JOH

Anesthesiology · 106d

Cleared Feb 11, 2003

1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR

K023793 · BTM

Anesthesiology · 90d

Cleared Feb 27, 2002

1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX

K014115 · BTM

Anesthesiology · 75d

Cleared Feb 13, 2002

HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE

K014073 · FMF

General Hospital · 65d

Cleared Mar 24, 1988

LARYNGECTOMY TUBE

K873992 · KAC

Ear, Nose, Throat · 175d

Cleared Jan 19, 1988

THERMOVENT 600, 1200, T, 02

JET VENTILATION ADAPTOR

ENDOBRONCHIAL TWIN LUMEN TUBE

K834565 · BTS

Anesthesiology · 20d

Cleared Jan 17, 1984

SWIVEL ADAPTOR W/ALARM PORT

K840015 · BZA

Anesthesiology · 13d

Portex, Inc. - FDA 510(k) Cleared Devices

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