Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Biotronik Cardiac Pacemakers — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K896184 | KALOS 05 PULSE GENERATOR | Biotronik Cardiac Pacemakers | 1990-01-18 | 85 | 0 |
| K894239 | NANOS | Biotronik Cardiac Pacemakers | 1989-11-01 | 134 | 0 |
| K894240 | NEOS 02 | Biotronik Cardiac Pacemakers | 1989-10-26 | 128 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda