Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Finnigan Corp. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K880418 | INCOS 50 MASS SPECTROMETER | Finnigan Corp. | 1988-05-31 | 120 | 0 |
| K880090 | ION TRAP DETECTOR | Finnigan Corp. | 1988-03-15 | 63 | 0 |
| K880089 | FINNIGAN MAT TSQ-70 | Finnigan Corp. | 1988-02-11 | 30 | 0 |
| K873603 | FINNIGAN MAT INCOS 50 | Finnigan Corp. | 1987-09-22 | 18 | 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