510(k) Report

FDA applicant

Perk Scientific, Inc.

Yeadon, PA1 decision2003–20030 recalls

FDA records 1 decision for Perk Scientific, Inc. (Yeadon, PA) in 2003: 1 510(k) clearance. All are in product code MRV (Drink, Glucose Tolerance). 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 Perk Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Perk Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Perk Scientific, Inc. 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?

  • MRVDrink, Glucose Tolerance1decision

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.

  • K032753Glucose Tolerance BeveragePerk Scientific, Inc. · 20031cites it

What has FDA decided for it lately?

  • K032753Glucose Tolerance BeveragePerk Scientific, Inc. · 2003

The one decision as Perk Scientific, Inc. →