Medical Device Manufacturer · US , Mchenry , IL

Bio-Med Devices, Inc. - FDA 510(k) Cleared Devices

14 submissions · 13 cleared · Since 1980

Total

Cleared

Denied

Bio-Med Devices, Inc. has 13 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Last cleared in 2022. Active since 1980.

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

Regulatory submissions have been managed by Bio-Med Devices C/O Promedic, LLC and ProMedic Consulting, LLC.

Bio-Med Devices, 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 - Bio-Med Devices, Inc.

14 devices

1-14 of 14

Anesthesiology · 203d

Cleared Sep 19, 1995

CROSSVENT-4 VENTILATOR

K942938 · CBK

Anesthesiology · 454d

Cleared Feb 12, 1990

IC-2A MRI ADULT/PEDIATRIC VENTILATOR

K896380 · CBK

Anesthesiology · 98d

Cleared Feb 12, 1990

MVP-10 MRI INFANT VENTILATOR

Anesthesiology · 136d

M-2 OXYGEN/TEMPERATURE MONITOR

K871337 · CCL

Anesthesiology · 63d

Cleared Apr 21, 1987

M-10 VENTILATION MONITOR

K871139 · CAP

Anesthesiology · 29d

Cleared Feb 09, 1983

PROGRAMMABLE VENTILATOR

K830230 · CBK

Anesthesiology · 12d

Cleared Feb 07, 1983

ET-3 EMERGENCY TRANSPORT VENTILATOR

Anesthesiology · 102d

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 18, 2026

Bio-Med Devices, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Bio-Med Devices, Inc.

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