# Litton Medical Electronics

- Location (FDA's records): Mchenry, IL
- FDA decisions: 38 (1982–1985): 38 510(k) clearances
- Product codes: DRT (17), DPS (5), DXJ (5), DSF (3), DSI (2), DXG (1), DPW (1), KLK (1), DSK (1), FLS (1), FLL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Access Battery, Inc.: 1 (https://510kreport.com/company/access-battery)

## Its most-cited devices
- K832015: Multiscriptor EK Various  #43 (1983), cited by 1

## Recent decisions
- K840522: Recomed Blood-Flow Meter H236-052-02 (May 16, 1985)
- K840899: Servomed Arrhycomp Central Monitor Sys (Nov 20, 1984)
- K840439: Recomed Cardiac Output Meter 236067- (Nov 20, 1984)
- K840523: Servomed Pulse Amplifier Module-206- (Oct 29, 1984)
- K840524: Servomed Basic Bedside Unit SMV 110TP (Oct 26, 1984)
- K840832: Servomed Oxcardiore Spirograph 324/111 (Sep 20, 1984)
- K840209: Servomed Medivision Scope SMV-235 (Sep 20, 1984)
- K832998: 2-Channel Recorder (Jun 1, 1984)

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