Medical Device Manufacturer · US , Mchenry , IL

Respiratory Care, Inc. - FDA 510(k) Cleared Devices

26 submissions · 26 cleared · Since 1976

Total

Cleared

Denied

Respiratory Care, Inc. has 26 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 26 cleared submissions from 1976 to 1989.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Respiratory Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Respiratory Care, Inc.

26 devices

1-12 of 26

Cleared Aug 28, 1989

RCI VIRAL/BACTERIAL FILTER

K892230 · CAH

General Hospital · 146d

Cleared Nov 21, 1988

MODIFIED CONCHATHERM III CONTROLLED HEATER

K884150 · BTT

Anesthesiology · 49d

Cleared Jun 21, 1988

CONCHATHERM III PLUS DUAL HEAT WIRE SERVO CONTROLL

CIRCAPAK UNIVERSAL VOLUME VENTILATOR CIRCUIT

K861555 · BZD

Anesthesiology · 41d

Cleared Jan 13, 1984

CONCHATHERM LHF HUMIDIFIER HEATER

K834151 · BTT

Anesthesiology · 43d

Cleared Dec 16, 1983

AQUAPAK 020 HUMIDIFIER ADAPTER

K833974 · BTT

Anesthesiology · 30d

Cleared Oct 27, 1983

SLIMB SINGLE LIMB BREATHING CIRCUIT

General Hospital · 33d

General Hospital · 20d

Respiratory Care, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Respiratory Care, Inc.

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