FDA applicant

Electro-Diagnostic Instruments

Burbank, CA4 decisions1982–19930 recalls

FDA records 4 decisions for Electro-Diagnostic Instruments (Burbank, CA) from 1982 to 1993: 4 510(k) clearances. Most are in product codes DSB (Plethysmograph, Impedance) and DPT (Probe, Blood-Flow, Extravascular). 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, cardiovascular panel, where it files most

How often FDA has decided Electro-Diagnostic Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electro-Diagnostic Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Electro-Diagnostic Instruments by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Electro-Diagnostic”

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

Electro-Nucleonics Laboratories, Inc. 41 Electro-Catheter Corp. 35 Electro-Biology, Inc. 28 Electro Medical Systems SA 11 Electro-Nucleonics, Inc. 9 Electro Therapeutic Devices, Inc. 8 Electro Med Supply, Inc. 8 Electro-Med Health Industries, Inc. 6 Electro Medical Systems (Ems Sa) 3 Electro Fiberoptics Corp. 3 Electro-Cap Intl., Inc. 3 Electro-Diagnostic Imaging, Inc. 2

Electro-Diagnostic Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Electro-Diagnostic”