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DLI — Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase Class I

FDA Device Classification

Classification Details

Product Code
DLI
Device Class
Class I
Regulation Number
862.3240
Submission Type
Review Panel
TX
Medical Specialty
Clinical Toxicology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K950180e.i. dupont de nemours and coDUPONT DIMENSION(R) PSEUDOCHOLINESTERASE METHODMarch 15, 1995
K930208heraeus kulzerCHOLINESTERASE METHOD FOR TECHNICON CHEM1/TECHNICOApril 20, 1993
K860350sterling diagnosticsSERUM CHOLINESTERASE REAGENT SETApril 24, 1986
K860641em diagnostic systemsEASY-TEST (CHE) REAGENT, ITEM NO. 67522/93April 3, 1986
K833062sterling biochemicalSERUM CHOLINESTERASE REAGENT SETNovember 25, 1983
K771024american monitorCHOLINESTERASE REAGENT SYSTEMJuly 15, 1977