Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Core-M, 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) |
|---|---|---|---|---|---|
| K960861 | OMICRON MONITOR, DELTA MONITOR | Core-M, Inc. | 1996-08-19 | 171 | 0 |
| K921978 | BREATH TRACKER(TM) MODEL 1800 CAN-O-GAUGE | Core-M, Inc. | 1992-11-17 | 203 | 0 |
| K892942 | BREATH TRACKER | Core-M, Inc. | 1989-06-23 | 63 | 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