Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Dufco Electronics, Inc. · Predicate Candidate Screening

4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K881463MULTIMODE(TM) POWER MODULE SYSTEMDufco Electronics, Inc.1988-07-181020
K881461MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH.Dufco Electronics, Inc.1988-07-181020
K881464MULTIMODE(TM) INTERFACE SYS. FOR EVEREST & JENNINGDufco Electronics, Inc.1988-07-181020
K881462UNIMODE(TM) POWER MODULE SYSTEMDufco Electronics, Inc.1988-07-181020

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda