# Angiomed GmbH & Co. Medizintechnik KG

- Location (FDA's records): Germany, DE
- FDA decisions: 1 (1992–1992): 1 510(k) clearance
- Product codes: KNW (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K912892: Auto-Vac Biopsy Needle (Feb 7, 1992)

Source page: https://510kreport.com/company/angiomed-co-medizintechnik