510(k) Report

FDA applicant

Delta Medical Electronics, Inc.

Walker, MI4 decisions1982–19830 recalls

FDA records 4 decisions for Delta Medical Electronics, Inc. (Walker, MI) from 1982 to 1983: 4 510(k) clearances. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). 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, general and plastic surgery panel, where it files most

How often FDA has decided Delta Medical Electronics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Delta Medical Electronics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Delta Medical Electronics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Delta”

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