# Arco Medical Products Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 21 (1976–1980): 21 510(k) clearances
- Product codes: DXY (15), DTD (2), DRT (1), DPS (1), DTB (1), IKY (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
- K802588: Model 3003 Unipolar Demand Cardiac Gen. (Nov 19, 1980)
- K801806: External Silastic Boot for Cardiac Pulse (Sep 9, 1980)
- K800837: Programmable Bipolar Cardiac Generator (Jun 30, 1980)
- K801241: Unipolar Programmable Lithium Card. Gen. (Jun 30, 1980)
- K800838: Arcolith 3022&Arcolith 3023 Cardiac Gen. (Jun 4, 1980)
- K800326: Arcolith 3021-Cardiac Pulse Generator (Mar 17, 1980)
- K792216: Arcolith 2100-Cardiac Pulse Generator (Nov 29, 1979)
- K792299: Arcolith 3020-Cardiac Pulse Generator (Nov 29, 1979)

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