Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Rlt Medical Assoc., 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) |
|---|---|---|---|---|---|
| K992772 | CARDIOPHONICS 1000 MEMORY MONITOR | Rlt Medical Assoc., Inc. | 1999-09-17 | 30 | 0 |
| K934975 | TELEPHONE ELECTROCARDIOGRAPH TRANSMITTER | Rlt Medical Assoc., Inc. | 1995-04-06 | 535 | 0 |
| K915224 | CARDIOPHONICS MEMORY TRANSMITTER | Rlt Medical Assoc., Inc. | 1992-02-07 | 79 | 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