# Siemens-Pacesetter, Inc.

- Location (FDA's records): Sylmar, CA
- FDA decisions: 7 (1992–1994): 7 510(k) clearances
- Product codes: DTB (6), DTD (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
- K942440: Afp Cardiac Pacing System Model 283 (Aug 8, 1994)
- K925038: Pacing Lead Model 1188T (Jul 15, 1994)
- K932892: Passive Plus Endocardial Pacing Leads Var. Models (Jul 6, 1994)
- K930876: Silicone Bipolar Lead Models 1136T, 1142T &1146T (Jun 15, 1994)
- K925347: Model 1148T Transvenous, Screw-in Lead (Jun 10, 1993)
- K920822: Cardiovascular Permanent Pacemaker Electrode (Jan 22, 1993)
- K921318: Adapting Sleeve Kit Model 4023 (Aug 3, 1992)

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