Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Siemens-Pacesetter with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 8, 1994: AFP CARDIAC PACING SYSTEM MODEL 283.
| Aug 8, 1994 | AFP CARDIAC PACING SYSTEM MODEL 283K942440 · DTB | 510(k) clearances |
| Jul 15, 1994 | PACING LEAD MODEL 1188TK925038 · DTB | 510(k) clearances |
| Jul 6, 1994 | PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELSK932892 · DTB | 510(k) clearances |
| Jun 15, 1994 | SILICONE BIPOLAR LEAD MODELS 1136T, 1142T &1146TK930876 · DTB | 510(k) clearances |
| Jun 10, 1993 | MODEL 1148T TRANSVENOUS, SCREW-IN LEADK925347 · DTB | 510(k) clearances |
| Jan 22, 1993 | CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODEK920822 · DTB | 510(k) clearances |
| Aug 3, 1992 | ADAPTING SLEEVE KIT MODEL 4023K921318 · DTD | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
