Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Oldelft Corp. of America

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K980296 OLDELFT DIGIDELCAKPR1998-04-17 View
510(k) K973219 AMBER DUKPR1997-10-08 View
510(k) K946128 SIMULIX-HPKPQ1995-05-12 View
510(k) K950037 N 800 HFIZO1995-02-15 View
510(k) K932848 SIMULIX-MC CT EXTENSIONJAK1994-03-22 View
510(k) K923584 THERAPAX DXT 300 SERIES 3JAD1993-01-15 View
510(k) K914784 PAPILLION PROCTOSCOPEKQA1992-06-05 View
510(k) K912466 OLDELFT SIMULIX-MCKPQ1991-06-28 View
510(k) K892659 ELECTRODELCAIZG1989-11-21 View
↑