# Argosy Electronics

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 24 (1993–1998): 24 510(k) clearances
- Product codes: ESD (24)
- 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
- K974242: Argosy Programmable Onque (Jan 20, 1998)
- K971699: Argosy Dynameq (Jul 3, 1997)
- K961729: Argosy Programmable (May 29, 1996)
- K954038: K-Amp 16, HI-Band K-Amp, Ultra Compression & Hearing Protection/Hearing Instrument (Sep 18, 1995)
- K952450: Wide Dynamic Range Compression with Active Tone Control (Jul 6, 1995)
- K952451: Class D Linear with Active Tone Control (Jul 6, 1995)
- K952452: Output Compression Limiter with Active Tone Control (Jul 6, 1995)
- K952453: Input Comprssion Limiter with Active Tone Control (Jun 21, 1995)

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