Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Technam, 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) |
|---|---|---|---|---|---|
| K801509 | HI-M-TEST FOR METHADONE TEST #2 | Technam, Inc. | 1980-07-14 | 14 | 0 |
| K800055 | H-I-M-TEST FOR DETECTING HUMAN CHOR. GON | Technam, Inc. | 1980-01-29 | 19 | 0 |
| K791551 | HI-M-TEST MORPHINE | Technam, Inc. | 1979-10-17 | 64 | 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