FDA 510(k) Applications for Medical Device Product Code "DLF"
(Enzyme Immunoassay, Ethosuximide)

FDA 510(k) Number Applicant Device Name Decision Date
K850174 ABBOTT LABORATORIES TDX ETHOSUXIMIDE 02/06/1985
K792584 E.I. DUPONT DE NEMOURS & CO., INC. "ACA" ETHOSURIMIDE TEST PACK 12/31/1979
K881607 EM DIAGNOSTIC SYSTEMS, INC. EASY-TEST EMIT(R) ETHOSUXIMIDE (ETHS) ITEM 16647 06/01/1988
K823801 MILES LABORATORIES, INC. AMES TDA ETHOSUXIMIDE TEST 01/14/1983
K823745 SYVA CO. ADVANCE EMIT-AED ETHOSUXIMIDE 01/07/1983
K780380 SYVA CO. ANALYZER, FAST, CENTRIFUGAL, GEMSAEC 04/12/1978
K780461 SYVA CO. ANALYZER-SUPPLEMENT, KINETIC, LKB 2086 04/12/1978
K844204 SYVA CO. EMIT QST ETHOSUXIMIDE ASSAY 12/11/1984
K832797 SYVA CO. MODIFICA- OF EMIT AED ETHOSUXIMIDE ASSAY 09/29/1983


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact