# Medicomp, Inc.

- Location (FDA's records): West Melbourne, FL
- FDA decisions: 23 (1983–2018): 23 510(k) clearances
- Product codes: DSI (7), CAI (2), DRG (2), DQK (2), DXH (2), BZA (2), MLO (1), BYD (1), BYL (1), BZD (1), CAH (1), DST (1)
- Predicates its devices cite: 5 (5 its own); citations of its devices by later devices: 8 (5 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
- Mercury Medical: 1 (https://510kreport.com/company/mercury-medical)
- Capintec, Inc.: 1 (https://510kreport.com/company/capintec)
- Airways Ltd., Inc.: 1 (https://510kreport.com/company/airways)

## Its most-cited devices
- K043454: Cardiopal AI with Diogenes SV (Cardiopal SV), Model PM410 (2005), cited by 2
- K830013: Epi Cardia Sys. - Ambulatory Monitor (1983), cited by 1
- K091696: Savi Wireless, Model PM500 (2009), cited by 1
- K861280: Medicomp Cpap Nasal Cannula (1986), cited by 1
- K090834: Epicardia 5000 (2009), cited by 1
- K851070: Resp-Bac Bacteria Filter (1985), cited by 1

## Recent decisions
- K173170: Epicardia Anywhere (Jan 10, 2018)
- K161916: TelePatch Cardiac Monitor (Dec 21, 2016)
- K091696: Savi Wireless, Model PM500 (Oct 26, 2009)
- K090834: Epicardia 5000 (May 15, 2009)
- K043454: Cardiopal AI with Diogenes SV (Cardiopal SV), Model PM410 (Mar 24, 2005)
- K981119: Cardiopal Model Number PM20 (Oct 14, 1998)
- K952846: Epicardia (Sep 18, 1995)
- K943915: Heat and Moisture Exchanger Filter (Hme) (Oct 14, 1994)

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