# Schwarzer Cardiotek GmbH

- Location (FDA's records): Heilbronn, DE
- FDA decisions: 1 (2019–2019): 1 510(k) clearance
- Product codes: DQK (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cardio Tek, BV: 1 (https://510kreport.com/company/cardio-tek)

## Firms that cite its devices most
- Cath Vision Aps: 1 (https://510kreport.com/company/cath-vision)
- Micropace Pty, Ltd.: 1 (https://510kreport.com/company/micropace)

## Its most-cited devices
- K183266: EP-TRACER System (2019), cited by 2

## Recent decisions
- K183266: EP-TRACER System (Mar 1, 2019)

Source page: https://510kreport.com/company/schwarzer-cardiotek