FDA applicant

Neotech Products, Inc.

Chatsworth, CA6 decisions1988–20020 recalls

FDA records 6 decisions for Neotech Products, Inc. (Chatsworth, CA) from 1988 to 2002: 6 510(k) clearances. Most are in product codes BSY (Catheters, Suction, Tracheobronchial) and BZA (Connector, Airway (Extension)). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Neotech Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neotech Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?