510(k) Report

FDA applicant

Dynatech Corp.

Mchenry, IL27 decisions1979–19910 recalls

FDA records 27 decisions for Dynatech Corp. (Mchenry, IL) from 1979 to 1991: 27 510(k) clearances. Most are in product codes LIB (Device, General Purpose, Microbiology…) and JTC (Device, Microtiter Diluting/Dispensing). 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, microbiology panel, where it files most

How often FDA has decided Dynatech Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dynatech Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dynatech 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 “Dynatech”

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