Medical Device Manufacturer · US , Mchenry , IL

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

27 submissions · 27 cleared · Since 1978

Total

Cleared

Denied

Hospitak, Inc. has 27 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 27 cleared submissions from 1978 to 1996.

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 - Hospitak, Inc.

27 devices

1-12 of 27

Cleared Feb 28, 1996

TRACH MASK MODEL (245, 246)

Anesthesiology · 105d

Cleared Aug 25, 1995

WARM N WET HME W/LUER ADAPTER

K953619 · BYD

Anesthesiology · 22d

Cleared Aug 25, 1995

WARM N WET HMEF W/LUER ADAPTER

K953620 · BYD

Anesthesiology · 22d

Cleared Nov 30, 1994

DISPOSABLE BACTERIAL BREATHNG FILTER

K915750 · CAH

General Hospital · 1077d

Cleared May 15, 1992

AEROSOL DELIVERY SYSTEMS

K920842 · LRD

Ear, Nose, Throat · 81d

Cleared Feb 11, 1992

DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL

K915228 · CCK

Anesthesiology · 83d

Cleared Oct 26, 1987

DISPOSABLE, MANUAL PULMONARY RESUSCITATOR

K873286 · BTM

Anesthesiology · 70d

Cleared Sep 19, 1985

INFLATABLE AIR SPLINTS

K853600 · FZF

General & Plastic Surgery · 23d

LOW PRESSURE ALARM FOR OXYGEN CYLINDER

K843212 · BXH

Anesthesiology · 35d

Cleared Apr 25, 1984

DISPOSABLE, HYPERBARIC OXYGEN CHAMBER

K840817 · KPJ

General & Plastic Surgery · 61d

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

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