Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Florence Medical , Ltd. · 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) |
|---|---|---|---|---|---|
| K020127 | SMARTFLOW PULSE TRANSMISSION COEFFICIENT | Florence Medical , Ltd. | 2002-02-14 | 30 | 0 |
| K012947 | SMARTFLOW | Florence Medical , Ltd. | 2001-10-02 | 28 | 0 |
| K003122 | SMARTFLOW, MODEL SFIP 2000 | Florence Medical , Ltd. | 2001-05-14 | 221 | 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