# Rudolf Medical GmbH + Co. KG

- Location (FDA's records): Mühlheim An Der Donau, DE
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 5 (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
- Guenter Bissinger Medizintechnik GmbH: 2 (https://510kreport.com/company/guenter-bissinger-medizintechnik)
- PAJUNK GmbH Medizintechnologie: 1 (https://510kreport.com/company/pajunk-medizintechnologie)
- Enable Medical Corp.: 1 (https://510kreport.com/company/enable-medical)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)

## Recent decisions
- K073498: Laparoscopic and Electrosurgical Instruments and Accessories, Laparoscopy Rudolf System (Sep 19, 2008)

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