510(k) Report

FDA applicant

Logos Scientific, Inc.

Mchenry, IL9 decisions1984–19900 recalls

FDA records 9 decisions for Logos Scientific, Inc. (Mchenry, IL) from 1984 to 1990: 9 510(k) clearances. Most are in product codes JJN (Apparatus, Electrophoresis, For Clinical Use) and JQT (Densitometer/Scanner (Integrating…). 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 Logos Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Logos Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Logos Scientific, Inc.’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 “Logos”

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