# Biosensor Corp.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 10 (1983–1999): 10 510(k) clearances
- Product codes: DQK (5), DSI (3), JAF (1), DPS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (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
- Braemar, Inc.: 3 (https://510kreport.com/company/braemar)
- Agilent Technologies, Inc.: 1 (https://510kreport.com/company/agilent-technologies)
- Lev-El, Ltd.: 1 (https://510kreport.com/company/lev-el)

## Its most-cited devices
- K950944: Ambulatory (Holter) Recording System (1996), cited by 4
- K974192: Biosensor Holter Monitor System (1998), cited by 1

## Recent decisions
- K990956: Biosensor Holter Monitor System Software, Model 1005 (Jun 14, 1999)
- K974192: Biosensor Holter Monitor System (Mar 4, 1998)
- K974546: Biosensor Holter Monitor System (Mar 4, 1998)
- K950944: Ambulatory (Holter) Recording System (Jun 18, 1996)
- K960449: PC Ecg 1200 Ecg and Stress Electrocardiography Testing System (Version 2.90) (May 30, 1996)
- K943338: Biosensor Bidop Vascular Test System (Apr 12, 1996)
- K950723: Ambulatory (Holter) Recording System (Feb 9, 1996)
- K922027: Ambulatory (Holter) Recording, Modification (Feb 17, 1993)

Source page: https://510kreport.com/company/biosensor