# Siemens Medical Laboratories, Inc.

- Location (FDA's records): Walnut Creek, CA
- FDA decisions: 13 (1979–1991): 13 510(k) clearances
- Product codes: IYE (9), DXK (1), JAD (1), LHN (1), JAI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 10 (0 its own)
- Recalls linked to its devices: 59 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Siemens Medical Solutions USA, Inc.: 6 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Aktina Medical Physics Corp.: 2 (https://510kreport.com/company/aktina-medical-physics)
- Intraop Medical, Inc.: 1 (https://510kreport.com/company/intraop-medical)
- American Biophysics, Inc.: 1 (https://510kreport.com/company/american-biophysics)

## Its most-cited devices
- K882729: Mevatron, M 2 Class (1988), cited by 3
- K910971: Z XT Radiation Therapy Treatment Table (1991), cited by 3
- K862339: Mevatron KD-2 (1986), cited by 2
- K852907: Siemens Mevatron ME (1985), cited by 1
- K903139: Beamview & Beamview Plus (Aka Project 743) (1990), cited by 1

## Recent decisions
- K910971: Z XT Radiation Therapy Treatment Table (May 3, 1991)
- K903139: Beamview & Beamview Plus (Aka Project 743) (Nov 7, 1990)
- K894230: Patient Data Management System (Project 735) (Aug 28, 1989)
- K882729: Mevatron, M 2 Class (Sep 19, 1988)
- K875272: Sonoline CF (Feb 18, 1988)
- K862339: Mevatron KD-2 (Oct 29, 1986)
- K854609: Mevamatic 3 (Feb 21, 1986)
- K852907: Siemens Mevatron ME (Sep 19, 1985)

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