Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Current Technologies, 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) |
|---|---|---|---|---|---|
| K833312 | ARTERIAL MICRO COLLECTION KIT | Current Technologies, Inc. | 1983-12-08 | 77 | 0 |
| K810816 | PREFILLED ARTERIAL BLOOD SAMPLING SYRING | Current Technologies, Inc. | 1981-04-07 | 14 | 0 |
| K802185 | ARTERIAL BLOOD SAMPLING KIT | Current Technologies, Inc. | 1980-10-10 | 30 | 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