FDA applicant
Delta Medical Electronics, Inc.
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
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.
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) ReportOther applicant names beginning “Delta”
FDA records each applicant name separately; these may or may not be the same firm.