# Artema Medical AB

- Location (FDA's records): Sweden, SE
- FDA decisions: 5 (1991–1995): 5 510(k) clearances
- Product codes: BYD (5)
- Predicates its devices cite: 0 (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 that cite its devices most
- Munktell Filter AB: 1 (https://510kreport.com/company/munktell-filter)

## Its most-cited devices
- K945359: Aqua+I-F, I-H, I-FH, II-H, II-FH, Iii-H (1995), cited by 1

## Recent decisions
- K945359: Aqua+I-F, I-H, I-FH, II-H, II-FH, Iii-H (Feb 21, 1995)
- K912333: Artema Aqua+ (Jul 26, 1991)
- K912336: Artema Aqua+ Flex (Jul 26, 1991)
- K912335: Artema Aqua+ N (Jul 26, 1991)
- K912334: Artema Aqua+ T & TS (Jul 26, 1991)

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