# Aequitron Medical, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 24 (1984–1997): 24 510(k) clearances
- Product codes: BZQ (9), CBK (4), DSH (3), HFM (2), KRC (1), CCL (1), CAW (1), LBI (1), DZD (1), DRT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Ilife Systems, Inc.: 1 (https://510kreport.com/company/ilife-systems)
- Bird Products Corp.: 1 (https://510kreport.com/company/bird-products)
- Pulmonetic Systems, Inc.: 1 (https://510kreport.com/company/pulmonetic-systems)
- Nellcor Puritan Bennett, Inc.: 1 (https://510kreport.com/company/nellcor-puritan-bennett)

## Its most-cited devices
- K905244: Model LP6 Ventilator, Modification (1990), cited by 2
- K903010: Continuous Volume Ventilator Model LP10 (1990), cited by 1
- K961972: Model Ami Infant Central Aphea/Heart Rate Monitor (1997), cited by 1

## Recent decisions
- K961972: Model Ami Infant Central Aphea/Heart Rate Monitor (Apr 18, 1997)
- K952880: Model LP-1000 Volume Ventilator (Jun 20, 1996)
- K944654: Oxygen Concentration Indicator (Nov 8, 1994)
- K914424: Model 6213 Remote Alarm (Sep 10, 1992)
- K915381: Portable Oxygen Generator (Mar 11, 1992)
- K911399: Nasal Cpap (Continuous Positive Air Pressure Syst) (Sep 19, 1991)
- K903020: Respiration/Heart Rate Monitor Model 9500/9550 (Apr 10, 1991)
- K905244: Model LP6 Ventilator, Modification (Nov 30, 1990)

Source page: https://510kreport.com/company/aequitron-medical