Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Upstream Peripheral Technologies — 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) |
|---|---|---|---|---|---|
| K120964 | UPSTREAM GR CATHETER | Upstream Peripheral Technologies | 2012-05-25 | 56 | 0 |
| K112887 | UPSTREAM NEEDLE HOLDER, UPSTREAM NEEDLE HOLDER WITH SHUT-OFF | Upstream Peripheral Technologies | 2012-03-21 | 173 | 0 |
| K112886 | UPSTREAM SUPPORT CATHETER | Upstream Peripheral Technologies | 2012-02-23 | 146 | 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