510(k) Report

FDA applicant

Advantage Medical Division of Cme Telemetrix

London, CA2 decisions1997–19980 recalls

FDA records 2 decisions for Advantage Medical Division of Cme Telemetrix (London, CA) from 1997 to 1998: 2 510(k) clearances. All are in product code IKN (Electromyograph, Diagnostic). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, physical medicine panel, where it files most

How often FDA has decided Advantage Medical Division of Cme Telemetrix’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advantage Medical Division of Cme Telemetrix since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advantage Medical Division of Cme Telemetrix by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Advantage”

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