Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medical Electronics Laboratories, Inc. · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K873533 | SIEMENS SIRECUST 1280, 1281 W/ARRHYTHMIA SOFTWARE | Medical Electronics Laboratories, Inc. | 1988-01-29 | 150 | 0 |
| K872249 | SIRECUST MODEL 960 AND 961 PATIENT MONITORING | Medical Electronics Laboratories, Inc. | 1987-07-21 | 39 | 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