# Acrostak (Schweiz) AG

- Location (FDA's records): Winterthur, CH
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: DQY (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)
- Asahi Intecc Co., Ltd.: 1 (https://510kreport.com/company/asahi-intecc)

## Recent decisions
- K171176: M-CATH Microcatheter (Sep 15, 2017)

Source page: https://510kreport.com/company/acrostak-schweiz