# Slk Medical GmbH

- Location (FDA's records): Waltrop, DE
- FDA decisions: 2 (2020–2021): 2 510(k) clearances
- Product codes: IRP (1), JOW (1)
- Predicates its devices cite: 2 (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 whose devices it cites most
- Mego Afek AC, Ltd.: 2 (https://510kreport.com/company/mego-afek-ac)

## Firms that cite its devices most
- Xiamen Weiyou Intelligent Technology Co., Ltd.: 1 (https://510kreport.com/company/xiamen-weiyou-intelligent-technology)

## Its most-cited devices
- K210913: V12 PRO (2021), cited by 1

## Recent decisions
- K210913: V12 PRO (Aug 4, 2021)
- K193476: VariLymph 12 pro (Aug 19, 2020)

Source page: https://510kreport.com/company/slk-medical