510(k) Report

FDA applicant

Technicon Instruments Corp.

Tarrytown, NY157 decisions1976–19910 recalls

FDA records 157 decisions for Technicon Instruments Corp. (Tarrytown, NY) from 1976 to 1991: 157 510(k) clearances. Most are in product codes JJC (Analyzer, Chemistry (Sequential Multiple…) and GKL (Counter, Cell, Automated (Particle Counter)). 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 Technicon Instruments Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Technicon Instruments Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Technicon”

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