# Cardiodata Corp.

- Location (FDA's records): Northborough, MA
- FDA decisions: 4 (1986–1990): 4 510(k) clearances
- Product codes: DSI (3), DSH (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
- Mortara Instrument, Inc.: 1 (https://510kreport.com/company/mortara-instrument)

## Its most-cited devices
- K900607: MK5 Detector & Alarm, Arrhythmia W/Software 2.11 (1990), cited by 1

## Recent decisions
- K900607: MK5 Detector & Alarm, Arrhythmia W/Software 2.11 (Oct 16, 1990)
- K881488: Holter Scanner (Sep 20, 1988)
- K873337: Model SSR1 Holter Monitor (Oct 9, 1987)
- K860167: Prodigy and Prodigy Plus (Mar 31, 1986)

Source page: https://510kreport.com/company/cardiodata