FDA applicant
Finnigan Corp.
FDA records 4 decisions for Finnigan Corp. (San Jose, CA) from 1987 to 1988: 4 510(k) clearances. Most are in product codes DOP (Mass Spectrometer, Clinical Use) and JJO (Flame Emission Photometer For Clinical Use). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Finnigan Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Finnigan Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Finnigan Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report