# Stierlen-Maquet AG

- Location (FDA's records): West Germany, GR
- FDA decisions: 10 (1984–1997): 10 510(k) clearances
- Product codes: JEB (4), GDC (3), FQO (2), BWN (1)
- 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
- Siemens Corp.: 1 (https://510kreport.com/company/siemens)

## Its most-cited devices
- K883613: Oper. Table for Percutan. Trans. Coronary Angio. (1988), cited by 1

## Recent decisions
- K970807: Mobile Operating Table 1132.01 (Mar 14, 1997)
- K926525: Betastar 1131.02 Mobile Operating Table (Oct 12, 1993)
- K920890: Operating Table System-Betamaquet 1140 (Jul 2, 1992)
- K883613: Oper. Table for Percutan. Trans. Coronary Angio. (Sep 15, 1988)
- K873276: Extension Device 1416 (Sep 17, 1987)
- K873274: Plaster Table 1418 (Sep 17, 1987)
- K873273: Orthopaedic Table 1420 (Sep 17, 1987)
- K873275: Extension Table 1417 (Sep 17, 1987)

Source page: https://510kreport.com/company/stierlen-maquet