# Life Science Instrumentation, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 20 (1981–1985): 20 510(k) clearances
- Product codes: DRT (10), LDD (7), DSI (1), DRX (1), DRO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K850812: Emergipace - External Pacemaker (Nov 5, 1985)
- K842037: LS 5 (Mar 1, 1985)
- K843396: LS-260G Monitor/Recorder & Defibillator (Oct 19, 1984)
- K840246: Mini-Defibrillator 280/4 (Apr 17, 1984)
- K822617: VPD540 Defibrillator (Apr 28, 1983)
- K831056: Defibrillator VPD 545 (Apr 28, 1983)
- K822616: LS6 Arrythmia Discriminator (Oct 18, 1982)
- K822615: Life Watch Lsi (Sep 21, 1982)

Source page: https://510kreport.com/company/life-science-instrumentation