510(k) Report

FDA applicant

Bioresource Technology, Inc.

Fort Lauderdale, FL4 decisions1995–20060 recalls

FDA records 4 decisions for Bioresource Technology, Inc. (Fort Lauderdale, FL) from 1995 to 2006: 4 510(k) clearances. Most are in product codes JJY (Multi-Analyte Controls, All Kinds (Assayed)) and GFS (Standards And Controls, Hemoglobin, Normal And…). 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 Bioresource Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bioresource Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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