510(k) Report

FDA applicant

Finnigan Corp.

San Jose, CA4 decisions1987–19880 recalls

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, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

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.

FIG. 1 — Finnigan Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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