510(k) Report

FDA applicant

Fisher Scientific Co., LLC

Mchenry, IL90 decisions1976–19930 recalls

FDA records 90 decisions for Fisher Scientific Co., LLC (Mchenry, IL) from 1976 to 1993: 89 510(k) clearances and 1 original PMA approval. Most are in product codes CHL (Electrode Measurement, Blood-Gases (Pco2, Po2)…) and JPK (Mixture, Hematology Quality Control). 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 Fisher Scientific Co., LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fisher Scientific Co., LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Fisher Scientific Co., LLC’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 “Fisher”

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