Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Telectronics and Cordis Pacing Systems — 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) |
|---|---|---|---|---|---|
| K883265 | MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD | Telectronics and Cordis Pacing Systems | 1988-10-14 | 74 | 0 |
| K881904 | CHANGE TO CATHODE POWDER SPECIFICATION | Telectronics and Cordis Pacing Systems | 1988-07-22 | 77 | 0 |
| K881711 | VICOR MODELS 410B & 410D AND MODIFIED 410A PACEMA. | Telectronics and Cordis Pacing Systems | 1988-05-26 | 36 | 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