Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Lifestream 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) |
|---|---|---|---|---|---|
| K033899 | LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUT | Lifestream Technologies, Inc. | 2004-05-20 | 155 | 0 |
| K000610 | RESOLUTION CHOLESTEROL MONITOR | Lifestream Technologies, Inc. | 2000-07-21 | 149 | 0 |
| K993096 | PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL M | Lifestream Technologies, Inc. | 1999-12-20 | 206 | 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