Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Cardio-Pace Medical, Inc. · 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) |
|---|---|---|---|---|---|
| K870142 | PINNACLE SR 8701 - UNIPOLAR & 8702 - BIPOLAR | Cardio-Pace Medical, Inc. | 1987-04-22 | 99 | 0 |
| K853771 | PINNACLE MULTI-PROGRAMMABLE PACING SYS | Cardio-Pace Medical, Inc. | 1986-07-15 | 309 | 0 |
| K853425 | CARIO-PACE DURAPULSE P101 COATED PULSE GENERATOR | Cardio-Pace Medical, Inc. | 1985-08-19 | 5 | 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