FDA applicant

Ametek/Thermox Instruments Division

Pittsburgh, PA2 decisions1988–19880 recalls

FDA records 2 decisions for Ametek/Thermox Instruments Division (Pittsburgh, PA) in 1988: 2 510(k) clearances. Most are in product codes BZL (Computer, Oxygen-Uptake) and CCL (Analyzer, Gas, Oxygen, Gaseous-Phase). 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 Ametek/Thermox Instruments Division’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ametek/Thermox Instruments Division since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ametek/Thermox Instruments Division by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Ametek/Thermox”

FDA records each applicant name separately; these may or may not be the same firm.

Ametek, Inc. 3

Ametek/Thermox Instruments Division

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ametek/Thermox”