FDA applicant
Diagnostic Products Corp.
FDA records 324 decisions for Diagnostic Products Corp. (Los Angeles, CA) from 1976 to 2006: 324 510(k) clearances. Most are in product codes DHB (System, Test, Radioallergosorbent (Rast)…) and CEW (Radioimmunoassay, Parathyroid Hormone). Its devices cite 65 predicates, 28 of them its own earlier devices. 57 recalls are linked to its devices.
FDA’s records also spell it “Diagnostic Products Corporation”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Diagnostic Products Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Diagnostic Products Corp. since 2007.
Recalls per year
3in 2025
Class I Class II/III not classified
Planning a device like Diagnostic Products Corp.’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 “Diagnostic”
FDA records each applicant name separately; these may or may not be the same firm.