Atlas FDA

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

Diagnostic Electronics Corp. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K861023DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLERDiagnostic Electronics Corp.1986-11-172440
K860651MICRON, MICROVASCULAR DOPPLERDiagnostic Electronics Corp.1986-07-181470
K830628REAL-TIME SPECTRUM ANALYZERDiagnostic Electronics Corp.1983-06-02930

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