510(k) Report

FDA applicant

Anthos Labtec Instruments

Washington, DC1 decision1993–19930 recalls

FDA records 1 decision for Anthos Labtec Instruments (Washington, DC) in 1993: 1 510(k) clearance. All are in product code JJQ (Colorimeter, Photometer, Spectrophotometer For…). 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 Anthos Labtec Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anthos Labtec Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • JJQColorimeter, Photometer, Spectrophotometer For Clinical Use1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K931907Anthos HT Readers, Including the Anthos HT II&IiiAnthos Labtec Instruments · 19932cite it

What has FDA decided for it lately?

  • K931907Anthos HT Readers, Including the Anthos HT II&IiiAnthos Labtec Instruments · 1993

The one decision as Anthos Labtec Instruments →

Other applicant names beginning “Anthos”

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

Anthos Labtec, Inc. 1