FDA applicant

Erie Scientific Co.

Portsmouth, NH1 decision1986–19860 recalls

FDA records 1 decision for Erie Scientific Co. (Portsmouth, NH) in 1986: 1 510(k) clearance. All are in product code KEO (Formulations, Paraffin, All). 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, pathology panel, where it files most

How often FDA has decided Erie Scientific Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Erie Scientific Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Erie Scientific Co.’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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Other applicant names beginning “Erie”

FDA records each applicant name separately; these may or may not be the same firm.

Erie Medical 5 Erie Controls 1 Erie Mfg., Co. 1

Erie Scientific Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Erie”