# Arbo Medical, Inc.

- Location (FDA's records): Stratford, CT
- FDA decisions: 15 (1989–1995): 15 510(k) clearances
- Product codes: DRX (7), DSA (3), CAH (2), FIB (1), JOT (1), FMT (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
- K940323: Arbo Diagnostic Ecg Patient Cables & Leadwires Arbo Shielded Multi-Lead Cable & Lead System (Apr 12, 1995)
- K935437: Arbo H85V/H87V/H27V Dispos Monit Electrodes (Apr 6, 1995)
- K942905: Disposable Temperature Probe Cover (Feb 27, 1995)
- K940302: Arbo Monitring Safety Cable & Lead Wire Systems/Arbo Unsheilded Safety Cable & Lead System (Nov 30, 1994)
- K940322: Arbo VS Monitor Cable & Leadwire System Arbo Shielded Safety Cable & Lead Wire (Nov 28, 1994)
- K935246: Arbo H49P, H59P Disposable Monitoring Electrodes (Nov 16, 1994)
- K935429: Arbo H90, H91, H135 Disposable Monitoring Electrodes (Nov 1, 1994)
- K935281: Arbo H87P, H85P, H27P Disposable Monitoring Electrodes (Sep 6, 1994)

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