# Bio-Med Devices, Inc.

- Location (FDA's records): Madison, CT
- FDA decisions: 14 (1980–2022): 14 510(k) clearances
- Product codes: CBK (9), CAP (2), CCL (2), BSK (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 6 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Maxtec, LLC: 1 (https://510kreport.com/company/maxtec)

## Firms that cite its devices most
- Maquet Critical Care AB: 2 (https://510kreport.com/company/maquet-critical-care)
- Draeger Medical Systems, Inc.: 1 (https://510kreport.com/company/draeger-medical-systems)
- Drager Medical B.V.: 1 (https://510kreport.com/company/drager-medical)
- Airon Corporation: 1 (https://510kreport.com/company/airon)

## Its most-cited devices
- K896380: IC-2A Mri Adult/Pediatric Ventilator (1990), cited by 2
- K896381: MVP-10 Mri Infant Ventilator (1990), cited by 2
- K942938: Crossvent-4 Ventilator (1995), cited by 2

## Recent decisions
- K213948: OxyMinder (Mar 17, 2022)
- K173973: TV-100 (Jul 20, 2018)
- K942938: Crossvent-4 Ventilator (Sep 19, 1995)
- K896380: IC-2A Mri Adult/Pediatric Ventilator (Feb 12, 1990)
- K896381: MVP-10 Mri Infant Ventilator (Feb 12, 1990)
- K873614: CBG Cuff Manometer (Jan 22, 1988)
- K871336: M-1 Pressure Monitor (Jun 5, 1987)
- K871337: M-2 Oxygen/Temperature Monitor (Jun 5, 1987)

Source page: https://510kreport.com/company/bio-med-devices