510(k) Report

FDA applicant

Teledyne Electronic Technologies

City Of Industry, CA2 decisions1999–20000 recalls

FDA records 2 decisions for Teledyne Electronic Technologies (City Of Industry, CA) from 1999 to 2000: 2 510(k) clearances. All are in product code 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 Teledyne Electronic Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Teledyne Electronic Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Teledyne”

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