FDA applicant

Victorch Meditek, Inc.

San Diego, CA2 decisions2001–20010 recalls

FDA records 2 decisions for Victorch Meditek, Inc. (San Diego, CA) in 2001: 2 510(k) clearances. Most are in product codes JHI (Visual, Pregnancy Hcg, Prescription Use) and DHA (System, Test, Human Chorionic Gonadotropin). 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 Victorch Meditek, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Victorch Meditek, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Victorch Meditek, Inc.

Which product codes does it file in?

What has FDA decided for it lately?