Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Hittman Medical Systems — 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) |
|---|---|---|---|---|---|
| K832772 | SATURN-24HR. HOLTER SCANNER | Hittman Medical Systems | 1983-11-03 | 79 | 0 |
| K791632 | COMPU-SCAN | Hittman Medical Systems | 1979-11-13 | 84 | 0 |
| K790300 | META III | Hittman Medical Systems | 1979-03-27 | 43 | 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