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DMR — Solution, M-Nitrophenol, Specific Reagent For Cholinesterase Class I

FDA Device Classification

Classification Details

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

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K790986	wampole laboratories	RF CONTROLS	June 28, 1979