FDA applicant

Metracor Technologies, Inc.

San Diego, CA1 decision2002–20020 recalls

FDA records 1 decision for Metracor Technologies, Inc. (San Diego, CA) in 2002: 1 510(k) clearance. All are in product code LZF (Pump, Infusion, Analytical Sampling). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Metracor Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Metracor Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?