# Micropace Pty, Ltd.

- Location (FDA's records): Canterbury, Nsw, AU
- FDA decisions: 3 (2002–2026): 3 510(k) clearances
- Product codes: JOQ (2), DQK (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 5 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Digital Cardiovascular Instruments, Inc.: 1 (https://510kreport.com/company/digital-cardiovascular-instruments)
- Schwarzer Cardiotek GmbH: 1 (https://510kreport.com/company/schwarzer-cardiotek)

## Firms that cite its devices most
- Mennen Medical, Inc.: 1 (https://510kreport.com/company/mennen-medical)
- Fischer Medical: 1 (https://510kreport.com/company/fischer-medical)
- St Cardio Technologies, LLC: 1 (https://510kreport.com/company/st-cardio-technologies)

## Its most-cited devices
- K011826: EPS320 Cardiac Stimulator (2002), cited by 4
- K072200: Stimlab (2007), cited by 1

## Recent decisions
- K253088: OneStim-DUO Cardiac Stimulator (MP5003-4CO) (Jun 12, 2026)
- K072200: Stimlab (Oct 26, 2007)
- K011826: EPS320 Cardiac Stimulator (Jan 24, 2002)

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