Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Trimline Medical Products Corp. · 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) |
|---|---|---|---|---|---|
| K092604 | LARGE FACE ANEROID SPHYGMOMANOMETER, WALL MODEL, DESK MODEL, | Trimline Medical Products Corp. | 2009-10-21 | 57 | 0 |
| K080189 | TEMPA-KUFF SOFT BLOOD PRESSURE CUFF, MODEL 39XXX ; VINYL,MOD | Trimline Medical Products Corp. | 2008-08-15 | 203 | 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