FDA applicant

Diagnostic Electronics Corp.

Lexington, MA3 decisions1983–19860 recalls

FDA records 3 decisions for Diagnostic Electronics Corp. (Lexington, MA) from 1983 to 1986: 3 510(k) clearances. Most are in product codes DPW (Flowmeter, Blood, Cardiovascular) and DXG (Computer, Diagnostic, Pre-Programmed…). 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 Diagnostic Electronics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diagnostic Electronics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Diagnostic”

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

Diagnostic Products Corp. 324 Diagnostic Systems Laboratories, Inc. 94 Diagnostic Chemicals, Ltd. (Usa) 77 Diagnostic Reagents, Inc. 66 Diagnostic Chemicals, Ltd. 66 Diagnostic Hybrids, Inc. 37 Diagnostic Technology, Inc. 28 Diagnostic Solutions, Inc. 26 Diagnostic Ultrasound Corp. 16 Diagnostic Systems 14 Diagnostic Reagent Tech. 10 Diagnostic Specialties 8

Diagnostic Electronics Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Diagnostic”