FDA applicant

Dynatech Laboratories, Inc.

Chantilly, VA44 decisions1978–19960 recalls

FDA records 44 decisions for Dynatech Laboratories, Inc. (Chantilly, VA) from 1978 to 1996: 44 510(k) clearances. Most are in product codes JJQ (Colorimeter, Photometer, Spectrophotometer For…) and JTC (Device, Microtiter Diluting/Dispensing). Its devices cite 2 predicates, 2 of them its own earlier devices. 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 Dynatech Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dynatech Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dynatech Laboratories, 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 “Dynatech”

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

Dynatech Corp. 27 Dynatech/Nevada, Inc. 6 Dynatech Cryomedical Co. 6 Dynatech Medical Products 5 Dynatech Research & Development Co. 2

Dynatech Laboratories, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Dynatech”