510(k) Report

FDA applicant

Anthos Labtec, Inc.

Frederick, MD1 decision1995–19950 recalls

FDA records 1 decision for Anthos Labtec, Inc. (Frederick, MD) in 1995: 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, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anthos Labtec, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Anthos Labtec, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • JJQColorimeter, Photometer, Spectrophotometer For Clinical Use1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K955077Anthos 2010 ReaderAnthos Labtec, Inc. · 19951cites it

What has FDA decided for it lately?

  • K955077Anthos 2010 ReaderAnthos Labtec, Inc. · 1995

The one decision as Anthos Labtec, Inc. →

Other applicant names beginning “Anthos”

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

Anthos Labtec Instruments 1