FDA applicant

Marvic Interpharma, Inc.

Palm Harbor, FL3 decisions1985–19860 recalls

FDA records 3 decisions for Marvic Interpharma, Inc. (Palm Harbor, FL) from 1985 to 1986: 3 510(k) clearances. Most are in product codes DCK (C-Reactive Protein, Antigen, Antiserum, And…) and CKB (Acid Phosphatase, Naphthyl Phosphate). 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, immunology panel, where it files most

How often FDA has decided Marvic Interpharma, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Marvic Interpharma, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Marvic Interpharma, Inc.

Which product codes does it file in?

What has FDA decided for it lately?